Substituted 3-phenylpyrazoles

ABSTRACT

3-phenylpyrazoles of formula I                    
     wherein 
     R 1  is cyano, alkyl or haloalkyl; 
     R 2  is cyano or is optionally halogenated alkyl, alkoxy, alkylthio, alkylsulfinyl or alkylsulfonyl; 
     R 3  is hydrogen, cyano, halogen, alkyl or haloalkyl; 
     R 4  is hydrogen or halogen; 
     R 5  is cyano, halogen, or is optionally halogenated alkyl or alkoxy; 
     R 6 , R 7  independently of one another are optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl or phenyl, optionally substituted alkylcarbonyl, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl or optionally halogenated alkylsulfonyl; 
     X is a chemical bond, —C≡C—, —CH 2 —CH(R 8 )— or —CH═C(R 8 )—, wherein R 8  is hydrogen, cyano, nitro, halogen, alkyl or haloalkyl; 
     Y is oxygen or sulfur; 
     their preparation and their use for controlling undesirable vegetation.

The present invention relates to novel substituted 3-phenylpyrazoles ofthe formula I

in which the variables have the following meanings:

R¹ is C₁-C₄-alkyl or C₁-C₄-haloalkyl;

R² is cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy,C₁-C₄-haloalkoxy, C₁-C₄-alkylthio, C₁-C₄-haloalkylthio,C₁-C₄-alkylsulfinyl, C₁-C₄-haloalkylsulfinyl, C₁-C₄-alkylsulfonyl orC₁-C₄-haloalkylsulfonyl;

R³ is hydrogen, cyano, halogen, C₁-C₄-alkyl or C₁-C₄-haloalkyl;

R⁴ is hydrogen or halogen;

R⁵ is cyano, halogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy orC₁-C₄-haloalkoxy;

R⁶, R⁷ independently of one another are C₁-C₆-alkyl, C₁-C₆-haloalkyl,hydroxy-C₁-C₄-alkyl, cyano-C₁-C₄-alkyl, C₁-C₄-alkoxy-C₁-C₄-alkyl,C₁-C₄-haloalkoxy-C₁-C₄-alkyl, C₃-C₄-alkenyloxy-C₁-C₄-alkyl,C₃-C₄-alkynyloxy-C₁-C₄-alkyl, C₃-C₈-cycloalkyloxy-C₁-C₄-alkyl,amino-C₁-C₄-alkyl, C₁-C₄-alkylamino-C₁-C₄-alkyl,di(C₁-C₄-alkyl)amino-C₁-C₄-alkyl, C₁-C₄-alkylthio-C₁-C₄-alkyl,C₁-C₄-haloalkylthio-C₁-C₄-alkyl, C₃-C₄-alkenylthio-C₁-C₄-alkyl,C₃-C₄-alkynylthio-C₁-C₄-alkyl, C₁-C₄-alkylsulfinyl-C₁-C₄-alkyl,C₁-C₄-haloalkyl-sulfinyl-C₁-C₄-alkyl,C₃-C₄o-alkenylsulfinyl-C₁-C₄-alkyl, C₃-C₄-alkynylsulfinyl-C₁-C₄-alkyl,C₁-C₄-alkylsulfonyl-C₁-C₄-alkyl, C₁-C₄-haloalkylsulfonyl-C₁-C₄-alkyl,C₃-C₄-alkenylsulfonyl-C₁-C₄-alkyl, C₃-C₄-alkynylsulfonyl-C₁-C₄-alkyl,C₃-C₆-alkenyl, cyano-C₃-C₆-alkenyl, C₃-C₆-haloalkyl, C₃-C₆-alkynyl,cyano-C₃-C₆-alkynyl, C₃-C₆-haloalkynyl, (C₁-C₄-alkyl)-carbonyl,(C₁-C₄-haloalkyl)carbonyl, (C₁-C₄-alkoxy)carbonyl, aminocarbonyl,(C₁-C₄-alkyl)aminocarbonyl, di(C₁-C₄-alkyl)aminocarbonyl,(C₁-C₄-alkoxy-C₁-C₄-alkyl)carbonyl, C₁-C₄-alkylsulfonyl,C₁-C₄-haloalkylsulfonyl, (C₁-C₄-alkyl)carbonyl-C₁-C₄-alkyl,(C₁-C₄-haloalkyl)carbonyl-C₁-C₄-alkyl,(C₃-C₈-cycloalkyl)carbonyl-C₁-C₄-alkyl, (C₁-C₄-alkoxy)imino-C₁-C₄-alkyl,(C₃-C₄-alkenyloxy) imino-C₁-C₄-alkyl, hydroxycarbonyl-C₁-C₄-alkyl,(C₁-C₄-alkoxy)carbonyl-C₁-C₄-alkyl which can have a (C₁-C₄-alkoxy)iminogroup attached to it, (C₁-C₄-haloalkoxy) carbonyl-C₁-C₄-alkyl,(C₁-C₄-alkylthio)carbonyl-C₁-C₄-alkyl, aminocarbonyl-C₁-C₄-alkyl,(C₁-C₄-alkylamino)carbonyl-C₁-C₄-alkyl,di(C₁-C₄-alkylamino)carbonyl-C₁-C₄-alkyl, C₃-C₈-cycloalkyl,C₃-C₈-cycloalkyl-C₁-C₄-alkyl, phenyl, phenyl-C₁-C₄-alkyl or 3- to7-membered heterocyclyl or heterocyclyl-C₁-C₄-alkyl, it being possible,if desired, for all cycloalkyl rings and heterocycles to contain acarbonyl or thiocarbonyl ring member, and it being possible for eachcycloalkyl, phenyl or heterocyclyl ring to be unsubstituted or to haveattached to it one to four substituents, in each case selected from thegroup consisting of cyano, nitro, amino, hydroxyl, carboxyl, halogen,C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy,C₁-C₄-alkylthio, C₁-C₄-haloalkylthio, C₁-C₄-alkylsulfonyl,C₁-C₄-haloalkylsulfonyl, (C₁-C₄-alkoxy)carbonyl, (C₁-C₄-alkyl)carbonyl,(C₁-C₄-haloalkyl)carbonyl, (C₁-C₄-alkyl)carbonyloxy,(C₁-C₄-haloalkyl)carbonyloxy and di(C₁-C₄-alkyl)amino;

X is a chemical bond, a 1,2-ethynediyl group or a group *—CH₂—CH(R⁸)— or*—CH═C(R⁸)— which is bonded to the phenyl ring via the bondcharacterized with an asterisk, where R⁸ is hydrogen, cyano, nitro,halogen, C₁-C₄-alkyl or C₁-C₄-haloalkyl;

Y is oxygen or sulfur;

and to the agriculturally useful salts of the compounds I.

Furthermore, the invention relates to

the use of these compounds I as herbicides,

herbicidal compositions which comprise the compounds I as activesubstances,

processes for the preparation of the compounds I and of herbicidalcompositions using the compounds I, and

methods of controlling undesirable vegetation using the compounds I.

Herbicidally active 3-phenylpyrazoles have already been described inEP-A 443 059, WO 92/06 962, JP-A 03/151 367, WO 92/02 509, WO 96/15 115,WO 95/32 188, WO 95/33 728, WO 96/01 254, WO 96/02518 and WO 96 40 643.

However, the herbicidal properties of the known herbicides are notalways entirely satisfactory with regard to the harmful plants.

It is an object of the present invention to provide novel herbicidallyactive compounds with which undesirable plants can be controlled betterthan was possible to date.

We have found that this object is achieved by the present substituted3-phenylpyrazoles of the formula I and by their herbicidal activity.

We have furthermore found herbicidal compositions which comprise thecompounds I and have a very good herbicidal activity. Moreover, we havefound processes for the preparation of these compositions and methods ofcontrolling undesirable vegetation using the compounds I.

Depending on the substitution pattern, the compounds of the formula Ican contain one or more chiral centers, in which case they are presentas enantiomer or diastereomer mixtures. Depending on the meaning of X,E/Z isomers are also possible. The invention relates both to the pureenantiomers or diastereomers and to mixtures of these.

Suitable amongst the agriculturally useful salts are mainly salts ofthose cations or the acid addition salts of those acids whose cations,or anions, respectively, do not adversely affect the herbicidal activityof the compounds I. Thus, especially suitable cations are the ions ofthe alkali metals, preferably sodium and potassium, of the alkalineearth metals, preferably calcium, magnesium and barium, and of thetransition metals, preferably manganese, copper, zinc and iron, and theammonium ion which, if desired, can have attached to it one to fourC₁-C₄-alkyl substituents and/or a phenyl or benzyl substituent,preferably diisopropylammonium, tetramethylammonium, tetrabutylammonium,trimethylbenzylammonium, furthermore phosphonium ions, sulfonium ions,preferably tri(C₁-C₄-alkyl)sulfonium and sulfoxonium ions, preferablytri(C₁-C₄-alkyl)sulfoxonium.

Anions of useful acid addition salts are principally chloride, bromide,fluoride, hydrogen sulfate, sulfate, dihydrogen phosphate, hydrogenphosphate, phosphate, nitrate, hydrogen carbonate, carbonate,hexafluorosilicate, hexafluorophosphate, benzoate, and the anions ofC₁-C₄-alkanoic acids, preferably formate, acetate, propionate andbutyrate.

The organic moieties mentioned for the substituents R¹ to R³ and R⁵ toR⁸ or as radicals on cycloalkyl, phenyl or heterocyclyl rings arecollective terms for individual enumerations of the individual groupmembers. All carbon chains, ie. all alkyl, haloalkyl, alkoxy,haloalkoxy, alkylthio, haloalkylthio, alkylsulfinyl, haloalkylsulfinyl,alkylsulfonyl, haloalkylsulfonyl, cyanoalkyl, hydroxyalkyl,hydroxycarbonylalkyl, aminoalkyl, aminocarbonylalkyl, phenylalkyl,heterocyclylalkyl, alkylcarbonyl, haloalkylcarbonyl, alkylcarbonyloxy,haloalkylcarbonyloxy, alkoxycarbonyl, haloalkoxycarbonyl,alkylthiocarbonyl, alkylamino, alkenyl, haloalkenyl, cyanoalkenyl,alkynyl, haloalkynyl, cyanoalkynyl, alkenyloxy, alkynyloxy, alkenylthio,alkynylthio, alkenylsulfinyl, alkynylsulfinyl, alkenylsulfonyl, andalkynylsulfonyl moieties may be straight-chained or branched.Halogenated substituents preferably have attached to them one to fiveidentical or different halogen atoms.

The meaning of halogen is in each case fluorine, chlorine, bromine oriodine, in particular fluorine or chlorine.

Other examples are:

C₁-C₄-alkyl: CH₃, C₂H₅, n-propyl, CH(CH₃)₂, n-butyl, 1-methyl-propyl,CH₂—CH(CH₃)₂ or C(CH₃)₂ or C(CH₃)₃, in particular CH₃ or C₂H₅;

C₁-C₆-alkyl: C₁-C₄-alkyl as mentioned above, or, for example, n-pentyl,1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl,1-ethylpropyl, n-hexyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl,1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl,1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl,2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl,2-ethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl,1-ethyl-1-methylpropyl and 1-ethyl-2-methylpropyl, in particular CH₃,C₂H₅, n-propyl, CH(CH₃)₂, n-butyl, C(CH₃)₃, n-pentyl or n-hexyl;

C₁-C₄: a C₁-C₄-alkyl radical as mentioned above which is partially orfully substituted by fluorine, chlorine, bromine and/or iodine, ie.CH₂Cl, CH(Cl)₂, C(Cl)₃, CH₂F, CHF₂, CF₃ CHFCl, CF(Cl)₂, CF₂Cl, Cf₂Br,1-fluoroethyl, 2-fluoroethyl, 2-chloroethyl, 2-bromoethyl, 2-iodoethyl,2,2-difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2-fluoroethyl,2-chlor-2,2-difluoroethyl, 2,2-dichloro-2-fluoroethyl,1,2-dichloroethyl, 2,2,2-trichloroethyl, pentafluoroethyl,2-fluoropropyl, 3-fluoropropyl, 2,2-difluoropropyl, 2,3-difluoropropyl,2-chloropropyl, 3-chloropropyl, 2,3-dichloropropyl, 2-bromopropyl,3-bromopropyl, 3,3,3-trifluoropropyl, 3,3,3-trichloropropyl,2,2,3,3,3-pentafluoropropyl, heptafluoropropyl,1-(fluoromethyl)-2-fluoroethyl, 1-(chloromethyl)-2-chloroethyl,1-(bromomethyl)-2-bromoethyl, 4-fluorobutyl, 4-chlorobutyl, 4-bromobutylor nonafluorobutyl, in particular chloromethyl, fluoromethyl,difluoromethyl, brifluoromethyl, 2-fluoroethyl, 2-chloroethyl,1,2-dichloroethyl, 2,2,2-trifluoroethyl or pentafluoroethyl;

C₁-C₆-haloalkyl: C₁-C₆-alkyl as mentioned above which is partially orfully substituted by fluorine, chlorine and/or bromine, ie. one of theabovementioned C₁-C₄-haloalkyl radicals or 5-fluoropentyl,5-chloropentyl, 5-bromopentyl, 5-iodopentyl, 5,5,5-trichloropentyl,undecafluoropentyl, 6-fluorohexyl, 6-chlorohexyl, 6-bromohexyl,6-iodohexyl, 6,6,6-trichlorohexyl or dodecafluorohexyl, in particularfluoromethyl, difluoromethyl, trifluoromethyl, chloromethyl,2-fluoroethyl, 2-chloroethyl or 2,2,2-trifluoroethyl;

C₃-C₈-cycloalkyl: cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl,cycloheptyl or cyclooctyl, in particular cyclopentyl or cyclohexyl;

C₃-C₈-cycloalkyl, which contains a carbonyl or thiocarbonyl ring member:for example cyclobutanon-2-yl, cyclobutanon-3-yl, cyclopentanon-2-yl,cyclopentanon-3-yl, cyclohexanon-2-yl, cyclohexanon-4-yl,cycloheptanon-2-yl, cyclooctanon-2yl, cyclobutanthion-2-yl,cyclobutanthion-2yl, cyclobutanthion-3-yl, cyclopentanthion-2-yl,cyclopentanthion-3-yl, cyclohexanthion-2-yl, cyclohexanthion-4-yl,cycloheptanthion-2-yl or cyclooctanthion-2-yl;

C₁-C₄-alkoxy: OCH₃, OC₂H₅, n-propoxy, OCH(CH₃)₂, n-butoxy,1-methylpropoxy, 2-methylpropoxy or OC(CH₃)₃, in particular OCH₃, OC₂H₅,OCH(CH₃)₂ or OC (CH₃)₃;

C₁-C₄-haloalkoxy: C₁-C₄-alkoxy as mentioned above which is partially orfully substituted by fluorine, chlorine, bromine and/or iodine, ie.OCH₂Cl, OCH(Cl)₂, OC(Cl)₃, OCH₂F, OCHF₂, OCF₃, OCHFCl, OCF(Cl)₂, OCF₂Cl,OCF₂Br, 1-fluoroethoxy, 2-fluoroethoxy, 2-bromoethoxy, 2-iodoethoxy,2,2-difluoroethoxy, 2,2,2-trifluoroethoxy, 2-chloro-2-fluoroethoxy,2-chloro-2,2-difluoroethoxy, 2,2-dichloro-2-fluoroethoxy,1,2-dichloroethoxy, 2,2,2-trichloroethoxy, pentafluoroethoxy,2-fluoropropoxy, 3-fluoropropoxy, 2-chloropropoxy, 3-chloropropoxy,2-bromopropoxy, 3-bromopropoxy, 2,2-difluoropropoxy,2,3-difluoropropoxy, 2,3-dichloropropoxy, 3,3,3-trifluoropropoxy,3,3,3-trichloropropoxy, 2,2,3,3,3-pentafluoropropoxy,heptafluoropropoxy, 1-(fluoromethyl)-2-fluoroethoxy,1-(chloromethyl)-2-chloroethoxy, 1-(bromomethyl)-2-bromoethoxy,4-fluorobutoxy, 4-chlorobutoxy, 4-bromobutoxy or non-afluorobutoxy, inparticular chloromethoxy, fluoromethoxy, difluoromethoxy,trifuloromethoxy, 2-fluoroethoxy, 2-chloroethoxy, 1,2-dichloroethoxy,2,2,2-trifluoroethoxy or pentafluoroethoxy;

C₁-C₄-alkylthio: SCH₃, SC₂H₅, n-propylthio, SCH(CH₃)₂, n-butylthio,1-methylpropylthio, 2-methylpropylthio or SC(CH₃)₃, in particular SCH₃or SC₂H₅;

C₁-C₄-haloalkylthio: C₁-C₄-alkylthio as mentioned above which ispartially or fully substituted by fluorine, chlorine, bromine and/oriodine, ie. SCH₂Cl, SCH(Cl)₂, SC(Cl)₃, SCH₂F, SCHF₂, SCF₃, SCHFCl,SCF(Cl)₂, SCF₂Cl, SCF₂Br, 1-fluoroethylthio, 2-fluoroethylthio,2-chloroethylthio, 2-bromoethylthio, 2-iodoethylthio,2,2-difluoroethylthio, 2,2,2-trifluoroethylthio, 1,2-dichloroethylthio,2,2,2-trichloroethylthio, 2-chloro-2-fluoroethylthio,2-chloro-2,2-difluoroethylthio, 2,2-dichloro-2-fluoroethylthio,pentafluoroethylthio, 2-fluoropropylthio, 3-fluoropropylthio,2-chloropropylthio, 3-chloropropylthio, 2-bromopropylthio,3-bromopropylthio, 2,2-difluoropropylthio, 2,3-difluoropropylthio,2,3-dichloropropylthio, 3,3,3-trifluoropropylthio,3,3,3-trichloropropylthio, 2,2,3,3,3-pentafluoropropylthio,heptafluoropropylthio, 1-(fluoromethyl)-2-fluoroethylthio,1-(chloromethyl)-2-chloroethylthio, 1-(bromomethyl)-2-bromoethylthio,4-fluorobutylthio, 4-chlorobutylthio, 4-bromobutylthio ornonafluorobutoxy, in particular chloromethylthio, fluoromethylthio,difluoromethylthio, trifluoromethylthio, 2-fluoroethylthio,2-chloroethylthio, 1,2-dichloroethylthio, 2,2,2-trifluoroethylthio orpentafluoroethylthio;

C₁-C₄-alkylsulfinyl: SOCH₃, SOC₂H₅, n-propylsulfinyl, SOCH(CH₃)₂,n-butylsulfinyl, 1-methylpropylsulfinyl, 2-methylpropylsulfinyl orSOC(CH₃)₃, in particular SOCH₃ or SOC₂H₅;

C₁-C₄-haloalkylsulfinyl: a C₁-C₄-alkylsulfinyl radical as mentionedabove which is partially or fully substituted by fluorine, chlorine,bromine and/or iodine, ie. chloromethylsulfinyl, dichloromethylsulfinyl,trichloromethylsulfinyl, fluoromethylsulfinyl, difluoromethylsulfinyl,trifluoromethylsulfinyl, chlorofluoromethylsulfinyl,dichlorofluoromethylsulfinyl, chlorodifluoromethylsulfinyl,2-fluoroethylsulfinyl, 2-chloroethylsulfinyl, 2-bromoethylsulfinyl,2-iodoethylsulfinyl, 2,2-difluoroethylsulfinyl,2,2,2-trifluoroethylsulfinyl, 2-chloro-2-fluoroethylsulfinyl,2-chloro-2,2-difluoroethylsulfinyl, 2,2-dichloro-2-fluoroethylsulfinyl,1,2-dichloroethylsulfinyl, 2,2,2-trichloroethylsulfinyl,pentafluoroethylsulfinyl, 2-fluoropropylsulfinyl,3-fluoropropylsulfinyl, 2,2-difluoropropylsulfinyl,2,3-difluoropropylsulfinyl, 2-chloropropylsulfinyl,3-chloropropylsulfinyl, 2,3-dichloropropylsulfinyl,2-bromopropylsulfinyl, 3-bromopropylsulfinyl,3,3,3-trifluoropropylsulfinyl, 3,3,3-trichloropropylsulfinyl,2,2,3,3,3-pentafluoropropylsulfinyl, heptafluoropropylsulfinyl,1-(fluoromethyl)-2-fluoroethylsulfinyl,1-(chloromethyl)-2-chloroethylsulfinyl,1-(bromoethyl)-2-bromoethylsulfinyl, 4-fluorobutylsulfinyl,4-chlorobutylsulfinyl, 4-bromobutylsulfinyl or nonafluorobutylsulfinyl,in particular chloromethylsulfinyl, fluoromethylsulfinyl,difluoromethylsulfinyl, trifluoromethylsulfinyl, 2-fluoroethylsulfinyl,2-chloroethylsulfinyl, 1,2-dichloroethylsulfinyl,2,2,2-trifluoroethylsulfinyl or pentafluoroethylsulfinyl;

C₁-C₄-alkylsulfonyl: SO₂CH₃, SO₂C₂H₅, n-propylsulfonyl, SO₂CH(CH₃)₂,n-butylsulfonyl, 1-methylpropylsulfonyl, 2-methylpropylsulfonyl orSO₂C(CH₃)₃, in particular SO₂CH₃ or SO₂C₂H₅;

C₁-C₄-haloalkylsulfonyl: a C₁-C₄-alkylsulfonyl radical as mentionedabove which is partially or fully substituted by fluorine, chlorine,bromine and/or iodine, ie. chloromethylsulfonyl, dichloromethylsulfonyl,trichloromethylsulfonyl, fluoromethylsulfonyl, difluoromethylsulfonyl,trifluoromethylsulfonyl, chlorofluoromethylsulfonyl,dichlorofluoromethylsulfonyl, chlorodifluoromethylsulfonyl,2-fluoroethylsulfonyl, 2-chloroethylsulfonyl, 2-bromoethylsulfonyl,2-iodoethylsulfonyl, 2,2-difluoroethylsulfonyl,2,2,2-trifluoroethylsulfonyl, 2-chloro-2-fluoroethylsulfonyl,2-chloro-2,2-difluoroethylsulfonyl, 2,2-dichloro-2-fluoroethylsulfonyl,1,2-dichloroethylsulfonyl, 2,2,2-trichloroethylsulfonyl,pentafluoroethylsulfonyl, 2-fluoropropylsulfonyl,3-fluoropropylsulfonyl, 2,2-difluoropropylsulfonyl,2,3-difluoropropylsulfonyl, 2-chloropropylsulfonyl,3-chloropropylsulfonyl, 2,3-dichloropropylsulfonyl,2-bromopropylsulfonyl, 3-bromopropylsulfonyl,3,3,3-trifluoropropylsulfonyl, 3,3,3-trichloropropylsulfonyl,2,2,3,3,3-pentafluoropropylsulfonyl, heptafluoropropylsulfonyl,1-(fluoromethyl)-2-fluoroethylsulfonyl,1-(chloromethyl)-2-chloroethylsulfonyl,1-(bromoethyl)-2-bromoethylsulfonyl, 4-fluorobutylsulfonyl,4-chlorobutylsulfonyl, 4-bromobutylsulfonyl, or nonafluorobutylsulfonyl,in particular chloromethylsulfonyl, fluoromethylsulfonyl,difluoromethylsulfonyl, trifluoromethylsulfonyl, 2-fluoroethylsulfonyl,2-chloroethylsulfonyl, 1,2-dichloroethylsulfonyl,2,2,2-trifluoroethylsulfonyl or pentafluoroethylsulfonyl;

cyano-C₁-C₄-alkyl: for example CH₂CN, 1-cyanoethyl, 2-cyanoethyl,1-cyanoprop-1-yl, 2-cyanprop-1-yl, 3-cyanoprop-1-yl, 1-cyanobut-1-yl,2-cyanobut-1-yl, 3-cyanobut-1-yl, 4-cyanobut-1-yl, 1-cyanobut-2-yl,2-cyanobut-2-yl, 3-cyanobut-2-yl, 4-cyanobut-2-yl, 1-(CH₂CN)-eth-1-yl,1-(CH₂CN)-1-(CH₃)-eth-1-yl or 1-(CH₂CN)-prop-1-yl, in particular CH₂CNor 2-cyanoethyl;

hydroxy-C₁-C₄-alkyl: for example CH₂OH, 1-hydroxyethyl, 2-hydroxyethyl,1-hydroxyprop-1-yl, 2-hydroxyprop-1-yl, 3-hydroxyprop-1-yl,1-hydroxybut-1-yl, 2-hydroxybut-1-yl, 3-hydroxybut-1-yl,4-hydroxybut-1-yl, 1-hydroxybut-2-yl, 2-hydroxybut-2-yl,3-hydroxybut-2-yl, 4-hydroxybut-2-yl, 1-(CH₂OH)eth-1-yl,1-(CH₂OH)-1-(CH₃)-eth-1-yl or 1-(CH₂OH)prop-1-yl, in particular CH₂OH or2-hydroxyethyl;

hydroxycarbonyl-C₁-C₄-alkyl: for example CH₂COOH, 1-(COOH)ethyl,2-(COOH)ethyl, 1-(COOH)prop-1-yl, 2-(COOH)prop-1-yl, 3-(COOH)prop-1-yl,1-(COOH)but-1-yl, 2-(COOH)but-1-yl, 3-(COOH)but-1-yl, 4-(COOH)but-1-yl,1-(COOH)but-2-yl, 2-(COOH)but-2-yl, 3-(COOH)but-2-yl, 4-(COOH)but-2-yl,1-(CH₂COOH)eth-1-yl, 1-(CH₂COOH)-1-(CH₃)-eth-1-yl or1-(CH₂COOH)prop-1-yl, in particular CH₂-COOH or 2-hydroxycarbonylethyl;

amino-C₁-C₄-alkyl: for example CH₂NH₂, 1-aminoethyl, 2-aminoethyl,1-aminoprop-1-yl, 2-aminoprop-1-yl, 3-aminoprop-1-yl, 1-aminobut-1-yl,2-aminobut-1-yl, 3-aminobut-1-yl, 4-aminobut-1-yl, 1-aminobut-2-yl,2-aminobut-2-yl, 3-aminobut-2-yl, 4-aminobut-2-yl, 1(CH₂NH₂)eth-1-yl,1-(CH₂NH₂)-1-(CH₃)-eth-1-yl or 1-(CH₂NH₂)prop-1-yl, in particular CH₂NH₂or 2-aminoethyl;

aminocarbonyl-C₁-C₄-alkyl: for example CH₂CONH₂, 1-(CONH₂)ethyl,2-(CONH₂)ethyl, 1-(CONH₂)prop-1-yl, 2-(CONH₂)prop-1-yl,3-(CONH₂)prop-1-yl, 1-(CONH₂)but-1-yl, 2-(CONH₂)but-1-yl,3-(CONH₂)but-1-yl, 4-(CONH₂)but-1-yl, 1-(CONH₂)but-2-yl,2-(CONH₂)but-2-yl, 3-(CONH₂)but-2-yl, 4-(CONH₂)but-2-yl,1-(CH₂CONH₂)eth-1-yl, 1-(CH₂CONH₂)-1-(CH₃)-eth-1-yl or1-(CH₂CONH₂)prop-1-yl, in particular CH₂CONH₂ or 2-aminocarbonylethyl;

phenyl-C₁-C₄-alkyl: benzyl, 1-phenylethyl, 2-phenylethyl,1-phenylprop-1-yl, 2-phenylprop-1-yl, 3-phenylprop-1-yl,1-phenylbut-1-yl, 2-phenylbut-1-yl, 3-phenylbut-1-yl, 4-phenylbut-1-yl,1-phenylbut-2-yl, 2-phenylbut-2-yl, 3-phenylbut-2-yl, 4-phenylbut-2-yl,1-(phenylmethyl)eth-1-yl, 1-(phenylmethyl)-1-(methyl)eth-1-yl or1-(phenylmethyl)prop-1-yl, in particular benzyl or 2-phenylethyl;

C₃-C₈-cycloalkyl-C₁-C₄-alkyl: cyclopropylmethyl, 1-cyclopropylethyl,2-cyclopropylethyl, 1-cyclopropylprop-1-yl, 2-cyclopropylprop-1-yl,3-cyclopropylprop-1-yl, 1-cyclopropylbut-1-yl, 2-cyclopropylbut-1-yl,3-cyclopropylbut-1-yl, 4-cyclopropylbut-1-yl, 1-cyclopropylbut-2-yl,2-cyclopropylbut-2-yl, 3-cyclopropylbut-2-yl, 4-cyclopropylbut-2-yl,1-(cyclopropylmethyl)eth-1-yl, 1-(cyclopropylmethyl)-1-(CH₃)eth-1-yl,1-(cyclopropylmethyl)prop-1-yl, cyclobutylmethyl, 1-cyclobutylethyl,2-cyclobutylethyl, 1-cyclobutylprop-1-yl, 2-cyclobutylprop-1-yl,3-cyclobutylprop-1-yl, 1-cyclobutylbut-1-yl, 2-cyclobutylbut-1-yl,3-cyclobutylbut-1-yl, 4-cyclobutylbut-1-yl, 1-cyclobutylbut-2-yl,2-cyclobutylbut-2-yl, 3-cyclobutylbut-2-yl, 4-cyclobutylbut-2-yl,1-(cyclobutylmethyl)eth-1-yl, 1-(cyclobutylmethyl)-1-(CH₃)eth-1-yl,1-(cyclobutylmethyl)prop-1-yl, cyclopentylmethyl, 1-cyclopentyl-ethyl,2-cyclopentylethyl, 1-cyclopentylprop-1-yl, 2-cyclopentylprop-1-yl,3-cyclopentylprop-1-yl, 1-cyclopentylbut-1-yl, 2-cyclopentylbut-1-yl,3-cyclopentylbut-1-yl, 4-cyclopentylbut-1-yl, 1-cyclopentylbut-2-yl,2-cyclopentylbut-2-yl, 3-cyclopentylbut-2-yl, 4-cyclopentylbut-2-yl,1-(cyclopentylmethyl)eth-1-yl, 1-(cyclopentylmethyl)-1-(CH₃)eth-1-yl,1-(cyclopentylmethyl)prop-1-yl, cyclohexylmethyl, 1-cyclohexylethyl,2-cyclohexylethyl, 1-cyclohexylprop-1-yl, 2-cyclohexylprop-1-yl,3-cyclohexylprop-1-yl, 1-cyclohexylbut-1-yl, 2-cyclohexylbut-1-yl,3-cyclohexylbut-1-yl, 4-cyclohexylbut-1-yl, 1-cyclohexylbut-2-yl,2-cyclohexylbut-2-yl, 3-cyclohexylbut-2-yl, 4-cyclohexylbut-2-yl,1-(cyclohexylmethyl)eth-1-yl, 1-(cyclohexylmethyl)-1-(CH₃)eth-1-yl,1-(cyclohexylmethyl)prop-1-yl, cycloheptylmethyl, 1-cycloheptyl-ethyl,2-cycloheptylethyl, 1-cycloheptylprop-1-yl, 2-cycloheptylprop-1-yl,3-cycloheptylprop-1-yl, 1-cycloheptylbut-1-yl, 2-cycloheptylbut-1-yl,3-cycloheptylbut-1-yl, 4-cycloheptylbut-1-yl, 1-cycloheptylbut-2-yl,2-cycloheptylbut-2-yl, 3-cycloheptylbut-2-yl, 4-cycloheptylbut-2-yl,1-(cycloheptylmethyl)eth-1-yl, 1-(cycloheptylmethyl)-1-(CH₃) eth-1-yl,1-(cycloheptylmethyl) prop-1-yl, cyclooctylmethyl, 1-cyclooctylethyl,2-cyclooctylethyl, 1-cyclooctylprop-1-yl, 2-cyclooctylprop-1-yl,3-cyclooctylprop-1-yl, 1-cyclooctylbut-1-yl, 2-cyclooctylbut-1-yl,3-cyclooctylbut-1-yl, 4-cyclooctylbut-1-yl, 1-cyclooctylbut-2-yl,2-cyclooctylbut-2-yl, 3-cyclooctylbut-2-yl, 4-cyclooctylbut-2-yl,1-(cyclooctylmethyl)eth-1-yl, 1-(cyclooctylmethyl)-1-(CH₃)eth-1-yl or1-(cyclooctylmethyl)prop-1-yl, in particular C₃-C₆-cycloalkylmethyl;

C₃-C₈-cycloalkyl-C₁-C₄-alkyl, which contains a carbonyl or thiocarbonylring member: for example cyclobutanon-2-ylmethyl,cyclobutanon-3-ylmethyl, cyclopentanon-2-ylmethyl,cyclopentanon-3-ylmethyl, cyclohexanon-2-ylmethyl,cyclohexanon-4-ylmethyl, cycloheptanon-2-ylmethyl,cyclooctanon-2-ylmethyl, cyclobutanethion-2-ylmethyl,cyclobutanethion-3-ylmethyl, cyclopentanethion-2-ylmethyl,cyclopentanethion-3-ylmethyl, cyclohexanethion-2-ylmethyl,cyclohexanethion-4-ylmethyl, cycloheptanethion-2-ylmethyl,cyclooctanethion-2-ylmethyl, 1-(cyclobutanon-2-yl)ethyl,1-(cyclobutanon-3-yl)ethyl, 1-(cyclopentanon-2-yl)ethyl,1-(cyclopentanon-3-yl)ethyl, 1-(cyclohexanon-2-yl)ethyl,1-(cyclohexanon-4-yl)ethyl, 1-(cycloheptanon-2-yl)ethyl,1-(cyclooctanon-2-yl)ethyl, 1-(cyclobutanethion-2-yl)ethyl,1-(cyclobutanethion-3-yl)ethyl, 1-(cyclopentanethion-2-yl)ethyl,1-(cyclopentanethion-3-yl)ethyl, 1-(cyclohexanethion-2-yl)ethyl,1-(cyclohexanethion-4-yl)ethyl, 1-(cycloheptanethion-2-yl)ethyl,1-(cyclooctanethion-2-yl)ethyl, 2-(cyclobutanon-2-yl)ethyl,2-(cyclobutanon-3-yl)ethyl, 2-(cyclopentanon-2-yl)ethyl,2-(cyclopentanon-3-yl)ethyl, 2-(cyclohexanon-2-yl)ethyl,2-(cyclohexanon-4-yl)ethyl, 2-(cycloheptanon-2-yl)ethyl,2-(cyclooctanon-2-yl)ethyl, 2-(cyclobutanethion-2-yl)ethyl,2-(cyclobutanethion-3-yl)ethyl, 2-(cyclopentanethion-2-yl)ethyl,2-(cyclopentanethion-3-yl)ethyl, 2-(cyclohexanethion-2-yl)ethyl,2-(cyclohexanethion-4-yl)ethyl, 2-(cycloheptanethion-2-yl)ethyl,2-(cyclooctanethion-2-yl)ethyl, 3-(cyclobutanon-2-yl)propyl,3-(cyclobutanon-3-yl)propyl, 3-(cyclopentanon-2-yl)propyl,3-(cyclopentanon-3-yl)propyl, 3-(cyclohexanon-2-yl)propyl,3-(cyclohexanon-4-yl)propyl, 3-(cycloheptanon-2-yl)propyl,3-(cyclooctanon-2-yl)propyl, 3-(cyclobutanethion-2-yl)propyl,3-(cyclobutanethion-3-yl)propyl, 3-(cyclopentanethion-2-yl)propyl,3-(cyclopentanethion-3-yl)propyl, 3-(cyclohexanethion-2-yl)propyl,3-(cyclohexanethion-4-yl)propyl, 3-(cycloheptanethion-2-yl)propyl,3-(cyclooctanethion-2-yl)propyl, 4-(cyclobutanon-2-yl)butyl,4-(cyclobutanon-3-yl)butyl, 4-(cyclopentanon-2-yl)butyl,4-(cyclopentanon-3-yl)butyl, 4-(cyclohexanon-2-yl)butyl,4-(cyclohexanon-4-yl)butyl, 4-(cycloheptanon-2-yl)butyl,4-(cyclooctanon-2-yl)butyl, 4-(cyclobutanethion-2-yl)butyl,4-(cyclobutanethion-3-yl)butyl, 4-(cyclopentanethion-2-yl)butyl,4-(cyclopentanethion-3-yl)butyl, 4-(cyclohexanethion-2-yl)butyl,4-(cyclohexanethion-4-yl)butyl, 4-(cycloheptanethion-2-yl)butyl or4-(cyclooctanethion-2-yl)butyl;

heterocyclyl-C₁-C₄-alkyl: heterocyclylmethyl, 1-(heterocyclyl)ethyl,2-(heterocyclyl)ethyl, 1-(heterocyclyl)prop-1-yl,2-(heterocyclyl)prop-1-yl, 3-(heterocyclyl)prop-1-yl,1-(heterocyclyl)but-1-yl, 2-(heterocyclyl)but-1-yl,3-(heterocyclyl)but-1-yl, 4-(heterocyclyl)but-1-yl,1-(heterocyclyl)but-2-yl, 2-(heterocyclyl)but-2-yl,3-(heterocyclyl)but-2-yl, 4-(heterocyclyl)but-2-yl,1-(heterocyclylmethyl)eth-1-yl, 1-(heterocyclylmethyl)-1-(CH₃)eth-1-ylor 1-(heterocyclylmethyl)prop-1-yl, in particular heterocyclylmethyl or2-(heterocyclyl)ethyl;

C₁-C₄-alkoxy-C₁-C₄-alkyl and the alkoxyalkyl moiety of(C₁-C₄-alkoxy-C₁C₄-alkyl)carbonyl: C₁-C₄-alkyl which is substituted byC₁-C₄-alkoxy as mentioned above, i.e. CH₂OCH₃, CH₂OC₂H₅,n-propoxymethyl, (1-methylethoxy)methyl, n-butoxymethyl,(1-methylpropoxy)methyl, (2-methylpropoxy)methyl,(1,1-dimethylethoxy)methyl, 2-(methoxy)ethyl, 2-(ethoxy)ethyl,2-(n-propoxy)ethyl, 2-(1-methylethoxy)ethyl, 2-(n-butoxy)ethyl,2-(1-methylpropoxy)ethyl, 2-(2-methylpropoxy)ethyl,2-(1,1-dimethylethoxy)ethyl, 2-(OCH₃)propyl, 2-(OC₂H₅)propyl,2-(n-propoxy)propyl, 2-(1-methylethoxy)propyl, 2-(n-butoxy)propyl,2-(1-methylpropoxy)propyl, 2-(2-methylpropoxy)propyl,2-(1,1-dimethylethoxy)propyl, 3-(OCH₃)propyl, 3-(OC₂H₅)propyl,3-(n-propoxy)propyl, 3-(1-methylethoxy)propyl, 3-(n-butoxy)propyl,3-(1-methylpropoxy)propyl, 3-(2-methylpropoxy)propyl,3-(1,1-dimethylethoxy)propyl, 2-(OCH₃)butyl, 2-(OC₂H₅)butyl,2-(n-propoxy)butyl, 2-(1-methylethoxy)butyl, 2-(n-butoxy)butyl,2-(1-methylpropoxy)butyl, 2-(2-methylpropoxy)butyl,2-(1,1-dimethylethoxy)butyl, 3-(OCH₃)butyl, 3-(OC₂H₅)butyl,3-(n-propoxy)butyl, 3-(1-methylethoxy)butyl, 3-(n-butoxy)butyl,3-(1-methylpropoxy)butyl, 3-(2-methylpropoxy)butyl,3-(1,1-dimethylethoxy)butyl, 4-(OCH₃)butyl, 4-(OC₂H₅)butyl,4-(n-propoxy)butyl, 4-(1-methylethoxy)butyl, 4-(n-butoxy)butyl,4-(1-methylpropoxy)butyl, 4-(2-methylpropoxy)butyl or4-(1,1-dimethylethoxy)butyl, in particular methoxymethyl or2-methoxyethyl;

(C₁-C₄-alkoxy)imino-C₁-C₄-alkyl: C₁-C₄-alkyl which is substituted byC₁-C₄-alkoxyimino, such as methoxyimino, ethoxyimino, n-propoxyimino,1-methylethoxyimino, n-butoxyimino, 1-methylpropoxyimino,2-methylpropoxyimino or 1,1-dimethylethoxyimino, in particularmethoxyimino or ethoxyimino, i.e. 2-(methoxyimino)ethyl,2-(ethoxyimino)ethyl, 2-(n-propoxyimino)ethyl,2-(1-methylethoxyimino)ethyl, 2-(n-butoxyimino)ethyl,2-(1-methylpropoxyimino)ethyl, 2-(2-methylpropoxyimino)ethyl,2-(1,1-dimethylethoxyimino)ethyl, 2-(methoxyimino)propyl,2-(ethoxyimino)propyl, 2-(n-propoxyimino)propyl,2-(1-methylethoxyimino)propyl, 2-(n-butoxyimino)propyl,2-(1-methylpropoxyimino)propyl, 2-(2-methylpropoxyimino)propyl,2-(1,1-dimethylethoxyimino)propyl, 3-(methoxyimino)propyl,3-(ethoxyimino)propyl, 3-(n-propoxyimino)propyl,3-(1-methylethoxyimino)propyl, 3-(n-butoxyimino)propyl,3-(1-methylpropoxyimino)propyl, 3-(2-methylpropoxyimino)propyl,3-(1,1-dimethylethoxyimino)propyl, 2-(methoxyimino)butyl,2-(ethoxyimino)butyl, 2-(n-propoxyimino)butyl,2-(1-methylethoxyimino)butyl, 2-(n-butoxyimino)butyl,2-(1-methylpropoxyimino)butyl, 2-(2-methylpropoxyimino)butyl,2-(1,1-dimethylethoxyimino)butyl, 3-(methoxyimino)butyl,3-(ethoxyimino)butyl, 3-(n-propoxyimino)butyl,3-(1-methylethoxyimino)butyl, 3-(n-butoxyimino)butyl,3-(1-methylpropoxyimino)butyl, 3-(2-methylpropoxyimino)butyl,3-(1,1-dimethylethoxyimino)butyl, 4-(methoxy)butyl,4-(ethoxyimino)butyl, 4-(n-propoxyimino)butyl,4-(1-methylethoxyimino)butyl, 4-(n-butoxyimino)butyl,4-(1-methylpropoxyimino)butyl, 4-(2-methylpropoxyimino)butyl or4-(1,1-dimethylethoxyimino)butyl, in particular 2-(methoxyimino)ethyl or2-(ethoxyimino)ethyl;

C₁-C₄-haloalkoxy-C₁-C₄-alkyl: C₁-C₄-alkyl which is substituted byC₁-C₄-haloalkoxy as mentioned above, e.g. 2-difluoromethoxy)ethyl,2-(trifluoromethoxy)ethyl or 2-(pentafluoroethoxy)ethyl;

C₃-C₈-cycloalkyloxy-C₁-C₄-alkyl: cyclopropyloxymethyl,1-cyclopropyloxyethyl, 2-cyclopropyloxyethyl, 1-cyclopropyloxyprop-1-yl,2-cyclopropyloxyprop-1-yl, 3-cyclopropyloxyprop-1-yl,1-cyclopropyloxybut-1-yl, 2-cyclopropyloxybut-1-yl,3-cyclopropyloxybut-1-yl, 4-cyclopropyloxybut-1-yl,1-cyclopropyloxybut-2-yl, 2-cyclopropyloxybut-2-yl,3-cyclopropyloxybut-2-yl, 3-cyclopropyloxybut-2-yl,4-cyclopropyloxybut-2-yl, 1-(cyclopropyloxymethyl)eth-1-yl,1-(cyclopropyloxymethyl)-1-(CH₃)eth-1-yl,1-(cyclopropylmethyloxy)prop-1-yl, cyclobutyloxymethyl,1-cyclobutyloxyethyl, 2-cyclobutyloxyethyl, 1-cyclobutyloxyprop-1-yl,2-cyclobutyloxyprop-1-yl, 3-cyclobutyloxyprop-1-yl,1-cyclobutyloxybut-1-yl, 2-cyclobutyloxybut-1-yl,3-cyclobutyloxybut-1-yl, 4-cyclobutyloxybut-1-yl,1-cyclobutyloxybut-2-yl, 2-cyclobutyloxybut-2-yl,3-cyclobutyloxybut-2-yl, 4-cyclobutyloxybut-2-yl,1-(cyclobutyloxymethyl)eth-1-yl,1-(cyclobutyloxymethyl)-1-(CH₃)eth-1-yl,1-(cyclobutyloxymethyl)prop-1-yl, cyclopentyloxymethyl,1-cyclopentyloxyethyl, 2-cyclopentyloxyethyl,1-cyclopentyloxy-prop-1-yl, 2-cyclopentyloxyprop-1-yl,3-cyclopentyloxyprop-1-yl, 1-cyclopentyloxybut-1-yl,2-cyclopentyloxybut-1-yl, 3-cyclopentyloxybut-1-yl,4-cyclopentyloxybut-1-yl, 1-cyclopentyloxybut-2-yl,2-cyclopentyloxybut-2-yl, 3-cyclopentyloxybut-2-yl,4-cyclopentyloxybut-2-yl, 1-(cyclopentyloxymethyl)eth-1-yl,1-(cyclopentyloxymethyl)-1-(CH₃)eth-1-yl,1-(cyclopentyloxymethyl)prop-1-yl, cyclohexyloxymethyl,1-cyclohexyloxyethyl, 2-cyclohexyloxyethyl, 1-cyclohexyloxyprop-1-yl,2-cyclohexyloxyprop-1-yl, 3-cyclohexyloxyprop-1-yl,1-cyclohexyloxybut-1-yl, 2-cyclohexyloxybut-1-yl,3-cyclohexyloxybut-1-yl, 4-cyclohexyloxybut-1-yl,1-cyclohexyloxybut-2-yl, 2-cyclohexyloxybut-2-yl,3-cyclohexyloxybut-2-yl, 4-cyclohexyloxybut-2-yl,1-(cyclohexyloxymethyl)eth-1-yl,1-(cyclohexyloxymethyl)-1-(CH₃)eth-1-yl,1-(cyclohexyloxymethyl)prop-1-yl, cycloheptyloxymethyl,1-cycloheptyloxyethyl, 2-cycloheptyloxyethyl, 1-cycloheptyloxyprop-1-yl,2-cycloheptyloxyprop-1-yl, 3-cycloheptyloxyprop-1-yl,1-cycloheptyloxybut-1-yl, 2-cycloheptyloxybut-1-yl,3-cycloheptyloxybut-1-yl, 4-cycloheptyloxybut-1-yl,1-cycloheptyloxybut-2-yl, 2-cycloheptyloxybut-2-yl,3-cycloheptyloxybut-2-yl, 4-cycloheptyloxybut-2-yl,1-(cycloheptyloxymethyl)eth-1-yl,1-(cycloheptyloxymethyl)-1-(CH₃)eth-1-yl,1-(cycloheptyloxymethyl)prop-1-yl, cyclooctyloxymethyl,1-cyclooctyloxyethyl, 2-cyclooctyloxyethyl, 1-cyclooctyloxyprop-1-yl,2-cyclooctyloxyprop-1-yl, 3-cyclooctyloxyprop-1-yl,1-cyclooctyloxybut-1-yl, 2-cyclooctyloxybut-1-yl,3-cyclooctyloxybut-1-yl, 4-cyclooctyloxybut-1-yl,1-cyclooctyloxybut-2-yl, 2-cyclooctyloxybut-2-yl,3-cyclooctyloxybut-2-yl, 4-cyclooctyloxybut-2-yl,1-(cyclooctyloxymethyl)eth-1-yl, 1-(cyclooctyloxymethyl)-1-(CH₃)eth-1-ylor 1-(cyclooctyloxymethyl)prop-1-yl, in particularC₃-C₆-cycloalkoxymethyl or 2-(C₃-C₆-cycloalkoxy)ethyl;

C₁-C₄-alkylthio-C₁-C₄-alkyl: C₁-C₄-alkyl which is substituted byC₁-C₄-alkylthio as mentioned above, i.e. CH₂SCH₃, CH₂SC₂H₅,n-propylthiomethyl, CH₂SCH(CH₃)₂, n-butylthiomethyl,(1-methylpropylthio)methyl, (2-methylpropylthio)methyl, CH₂SC(CH₃)₃,2-methylthioethyl, 2-ethylthioethyl, 2-(n-propylthio)ethyl,2-(1-methylethylthio)ethyl, 2-(n-butylthio)ethyl,2-(1-methylpropylthio)ethyl, 2-(2-methylpropylthio)ethyl,2-(1,1-dimethylethylthio)ethyl, 2-(SCH₃)propyl, 3-(SCH₃)propyl,2-(SC₂H₅)propyl, 3-(SC₂H₅)propyl, 3-(propylthio)propyl,3-(butylthio)propyl, 4-(SCH₃)butyl, 4-(SC₂H₅)butyl,4-(n-propylthio)butyl or 4-(n-butylthio)butyl, in particular CH₂SCH₃ or2-(methylthio)ethyl;

C₁-C₄-haloalkylthio-C₁-C₄-alkyl: C₁-C₄-alkyl which is substituted byC₁-C₄-haloalkylthio as mentioned above, i.e.2-(difluoromethylthio)ethyl, 2-(trifluoromethylthio)ethyl or2-(pentafluoroethylthio)ethyl;

C₁-C₄-alkylsulfinyl-C₁-C₄-alkyl: C₁-C₄-alkyl which is substituted byC₁-C₄-alkylsulfinyl as mentioned above, i.e. CH₂SOCH₃, CH₂SOC₂H₅,n-propylsulfinylmethyl, (1-methylethylsulfinyl)methyl,n-butylsulfinylmethyl, (1-methylpropylsulfinyl)methyl,(2-methylpropylsulfinyl)methyl, (1,1-dimethylethylsulfinyl)methyl,2-methylsulfinylethyl, 2-ethylsulfinylethyl, 2-(n-propylsulfinyl)ethyl,2-(1-methylethylsulfinyl)ethyl, 2-(n-butylsulfinyl)ethyl,2-(1-methylpropylsulfinyl)ethyl, 2-(2-methylpropylsulfinyl)ethyl,2-(1,1-dimethylethylsulfinyl)ethyl, 2-(SOCH₃)propyl, 3-(SOCH₃)propyl,2-(SOC₂H₅)propyl, 3-(SOC₂H₅)propyl, 3-(propylsulfinyl)propyl,3-(butylsulfinyl)propyl, 4-(SOCH₃)butyl, 4-(SOC₂H₅)butyl,4-(n-propylsulfinyl)butyl or 4-(n-butylsulfinyl)butyl, in particular2-(SOCH₃)ethyl;

C₁-C₄-haloalkylsulfinyl-C₁-C₄-alkyl: C₁-C₄-alkyl which is substituted byC₁-C₄-haloalkylsulfinyl as mentioned above, i.e.2-(2,2,2-trifluoroethylsulfinyl)ethyl;

C₁-C₄-alkylsulfonyl-C₁-C₄-alkyl: C₁-C₄-alkyl which is substituted byC₁-C₄-alkylsulfonyl as mentioned above, i.e. CH₂SO₂CH₃, CH₂SO₂C₂H₅,n-propylsulfonylmethyl, (1-methylethylsulfonyl)methyl,n-butylsulfonylmethyl, (1-methylpropylsulfonyl)methyl,(2-methylpropylsulfonyl)methyl, (1,1-dimethylethylsulfonyl)methyl,2-methylsulfonylethyl, 2-ethylsulfonylethyl, 2-(n-propylsulfonyl)ethyl,2-(1-methylethylsulfonyl)ethyl, 2-(n-butylsulfonyl)ethyl,2-(1-methylpropylsulfonyl)ethyl, 2-(2-methylpropylsulfonyl)ethyl,2-(1,1-dimethylethylsulfonyl)ethyl, 2-(SO₂CH₃)propyl, 3-(SO₂CH₃)propyl,2-(SO₂C₂H₅)propyl, 3-(SO₂C₂H₅)propyl, 3-(propylsulfonyl)propyl,3-(butylsulfonyl)propyl, 4-(SO₂CH₃)butyl, 4-(SO₂C₂H₅)butyl,4-(n-propylsulfonyl)butyl or 4-(n-butylsulfonyl)butyl, in particular2-(SO₂CH₃)ethyl or 2-(SO₂C₂H₅)ethyl;

C₁-C₄-haloalkylsulfonyl-C₁-C₄-alkyl: C₁-C₄-alkyl which is substituted byC₁-C₄-haloalkylsulfonyl as mentioned above, i.e.2-(2,2,2-trifluoroethylsulfonyl)ethyl;

(C₁-C₄-alkyl)carbonyl: COCH₃, COC₂H₅, n-propylcarbonyl, COCH(CH₃)₂,n-butylcarbonyl, 1-methylpropylcarbonyl, 2-methylpropylcarbonyl orCOC(CH₃)₃, in particular COCH₃, COC₂H₅ or COC(CH₃)₃;

(C₁-C₄-haloalkyl)carbonyl: (C₁-C₄-alkyl)carbonyl as mentioned abovewhich is partially or fully substituted by fluorine, chlorine, bromineand/or iodine, i.e. COCH₂Cl, COCH(Cl)₂, COC(Cl)₃, COCH₂F, COCHF₂, COCF₃,COCHFCl, COCF(Cl)₂, COCF₂Cl, COCF₂Br, 1-fluoroethylcarbonyl,2-fluoroethylcarbonyl, 2,2-difluoroethylcarbonyl,2,2,2-trifluoroethylcarbonyl, 2-chloro-2-fluoroethylcarbonyl,2-chloro-2,2-difluoroethylcarbonyl, 2,2-dichloro-2-fluoroethylcarbonyl,1,2-dichloroethylcarbonyl, 2,2,2-trichloroethylcarbonyl, COC₂F₅,3-chloropropylcarbonyl, heptafluoropropylcarbonyl,1-(fluoromethyl)-2-fluoroethylcarbonyl,1-(chloromethyl)-2-chloroethylcarbonyl,1-(bromomethyl)-2-bromoethylcarbonyl, 4-fluorobutylcarbonyl,4-chlorobutylcarbonyl, 4-bromobutylcarbonyl or nonafluorobutylcarbonyl,in particular COCH₂Cl, COCH₂F, COCHF₂, COCF₃, 2-fluoroethylcarbonyl,2-chloroethylcarbonyl, 1,2-dichloroethylcarbonyl,2,2,2-trifluoroethylcarbonyl or COC₂F₅;

(C₁-C₄-alkyl)carbonyl-C₁-C₄-alkyl: C₁-C₄-alkyl which is substituted by(C₁-C₄-Alkyl)carbonyl as mentioned above, i.e. CH₂COCH₃, CH₂COC₂H₅ orCH₂COC(CH₃)₃;

(C₁-C₄-haloalkyl)carbonyl-C₁-C₄-alkyl: C₁-C₄-alkyl which is substitutedby (C₁-C₄-haloalkyl)carbonyl as mentioned above, i.e. CH₂COCF₃ orCH₂COCH₂Cl;

(C₃-C₈-cycloalkyl)carbonyl-C₁-C₄-alkyl: cyclopropyl-CO-CH₂-,1-(cyclopropyl-CO-)ethyl, 2-(cyclopropyl-CO-)ethyl,1-(cyclopropyl-CO-)prop-1-yl, 2-(cyclopropyl-CO-)prop-1-yl,3-(cyclopropyl-CO-)prop-1-yl, 1-(cyclopropyl-CO-)but-1-yl,2-(cyclopropyl-CO-)but-1-yl, 3-(cyclopropyl-CO-)but-1-yl,4-(cyclopropyl-CO-)but-1-yl, 1-(cyclopropyl-CO-)but-2-yl,2-(cyclopropyl-CO-)but-2-yl, 3-(cyclopropyl-CO-)but-2-yl,4-(cyclopropyl-CO-)but-2-yl, 1-(cyclopropyl-CO-CH₂-)eth-1-yl,1-(cyclopropyl-CO-CH₂-)-1-(CH₃)eth-1-yl,1-(cyclopropyl-CO-CH₂-)prop-1-yl, cyclobutyl-CO-CH₂-,1-(cyclobutyl-CO-)ethyl, 2-(cyclobutyl-CO-)ethyl,1-(cyclobutyl-CO-)prop-1-yl, 2-(cyclobutyl-CO-)prop-1-yl,3-(cyclobutyl-CO-)prop-1-yl, 1-(cyclobutyl-CO-)but-1-yl,2-(cyclobutyl-CO-)but-1-yl, 3-(cyclobutyl-CO-)but-1-yl,4-(cyclobutyl-CO-)but-1-yl, 1-(cyclobutyl-CO-)but-2-yl,2-(cyclobutyl-CO-)but-2-yl, 3-(cyclobutyl-CO-)but-2-yl,4-(cyclobutyl-CO-)but-2-yl, 1-(cyclobutyl-CO-CH₂-)eth-1-yl,1-(cyclobutyl-CO-CH₂-)-1-(CH₃)eth-1-yl, 1-(cyclobutyl-CO-CH₂-)prop-1-yl,cyclopentyl-CO-CH₂-, 1-(cyclopentyl-CO-)ethyl, 2-(cyclopentyl-CO-)ethyl,1-(cyclopentyl-CO-)prop-1-yl, 2-(cyclopentyl-CO-)prop-1-yl,3-(cyclopentyl-CO-)prop-1-yl, 1-(cyclopentyl-CO-)but-1-yl,2-(cyclopentyl-CO-)but-1-yl, 3-(cyclopentyl-CO-)but-1-yl,4-(cyclopentyl-CO-)but-1-yl, 1-(cyclopentyl-CO-)but-2-yl,2-(cyclopentyl-CO-)but-2-yl, 3-(cyclopentyl-CO-)but-2-yl,4-(cyclopentyl-CO-)but-2-yl, 1-(cyclopentyl-CO-CH₂-)eth-1-yl,1-(cyclopentyl-CO-CH₂-)-1-(CH₃)-eth-1-yl,1-(cyclopentyl-CO-CH₂-)prop-1-yl, cyclohexyl-CO-CH₂-,1-(cyclohexyl-CO-)ethyl, 2-(cyclohexyl-CO-)ethyl,1-(cyclohexyl-CO-)prop-1-yl, 2-(cyclohexyl-CO-)prop-1-yl,3-(cyclohexyl-CO-)prop-1-yl, 1-cyclohexyl-CO-)but-1-yl,2-(cyclohexyl-CO-)but-1-yl, 3-(cyclohexyl-CO-)but-1-yl,4-(cyclohexyl-CO-)but-1-yl, 1-(cyclohexyl-CO-)but-2-yl,2-(cyclohexyl-CO-)but-2-yl, 3-(cyclohexyl-CO-)but-2-yl,4-(cyclohexyl-CO-)but-2-yl, 1-(cyclohexyl-CO-CH₂-)eth-1-yl,1-(cyclohexyl-CO-CH₂-)-1-(CH₃)eth-1-yl, 1-(cyclohexyl-CO-CH₂-)prop-1-yl,cycloheptyl-CO-CH₂-, 1-(cycloheptyl-CO-)ethyl, 2-(cycloheptyl-CO-)ethyl,1-(cycloheptyl-CO-)prop-1-yl, 2-(cycloheptyl-CO-)prop-1-yl,3-(cycloheptyl-CO-)prop-1-yl, 1-(cycloheptyl-CO-)but-1-yl,2-(cycloheptyl-CO-)but-1-yl, 3-(cycloheptyl-CO-)but-1-yl,4-(cycloheptyl-CO-)but-1-yl, 1-(cycloheptyl-CO-)but-2-yl,2-(cycloheptyl-CO-)but-2-yl, 3-(cycloheptyl-CO-)but-2-yl,4-(cycloheptyl-CO-)but-2-yl, 1-(cycloheptyl-CO-CH₂-)eth-1-yl,1-(cycloheptyl-CO-CH₂-)-1-(CH₃)eth-1-yl,1-(cycloheptyl-CO-CH₂-)prop-1-yl, cyclooctyl-CO-CH₂-,1-(cyclooctyl-CO-)ethyl, 2-(cyclooctyl-CO-)ethyl,1-(cyclooctyl-CO-)prop-1-yl, 2-(cyclooctyl-CO-)prop-1-yl,3-(cyclooctyl-CO-)prop-1-yl, 1-(cyclooctyl-CO-)but-1-yl,2-(cyclooctyl-CO-)but-1-yl, 3-(cyclooctyl-CO-)but-1-yl,4-(cyclooctyl-CO-)but-1-yl, 1-(cyclooctyl-CO-)but-2-yl,2-(cyclooctyl-CO-)but-2-yl, 3-(cyclooctyl-CO-)but-2-yl,4-(cyclooctyl-CO-)but-2-yl, 1-(cyclooctyl-CO-CH₂-)eth-1-yl,1-(cyclooctyl-CO-CH₂-)-1-(CH₃)eth-1-yl or1-(cyclooctyl-CO-CH₂)prop-1-yl, in particular(C₃-C₆-cycloalkyl)carbonylmethyl;

C₁-C₄-alkylcarbonyloxy: O—COCH₃, O—COC₂H₅, n-propylcarbonyloxy,O—COCH(CH₃)₂, n-butylcarbonyloxy, 1-methylpropylcarbonyloxy,2-methylpropylcarbonyloxy or O—COC(CH₃)₃, in particular O—COCH₃,O—COC₂H₅ or O—COC(CH₃)₃;

(C₁-C₄-haloalkyl)carbonyloxy: (C₁-C₄-alkyl)carbonyloxy as mentionedabove which is partially or fully substituted by fluorine, chlorine,bromine and/or iodine, i.e. O—COCH₂Cl, O—COCH(Cl)₂, O—COC(Cl)₃,O—COCH₂F, O—COCHF₂, O—COCF₃, O—COCHFCl, O—COCF(Cl)₂, O—COCF₂Cl,O—COCF₂Br, 1-fluoroethylcarbonyloxy, 2-fluoroethylcarbonyloxy,2,2-difluoroethylcarbonyloxy, 2,2,2-trifluoroethylcarbonyloxy,2-chloro-2-fluoroethylcarbonyloxy,2-chloro-2,2-difluoroethylcarbonyloxy,2,2-dichloro-2-fluoroethylcarbonyloxy, 1,2-dichloroethylcarbonyloxy,2,2,2-trichloroethylcarbonyloxy, O—COC₂F₅, 3-chloropropylcarbonyloxy,heptafluoropropylcarbonyloxy, 1-(fluoromethyl)-2-fluoroethylcarbonyloxy,1-(chloromethyl)-2-chloroethylcarbonyloxy,1-(bromomethyl)-2-bromoethylcarbonyloxy, 4-fluorobutylcarbonyloxy,4-chlorobutylcarbonyloxy, 4-bromobutylcarbonyloxy ornonafluorobutylcarbonyloxy, in particular O—COCH₂Cl, O—COCH₂F, O—COCHF₂,O—COCF₃, 2-fluoroethylcarbonyloxy, 2-chloroethylcarbonyloxy,1,2-dichloroethylcarbonyloxy, 2,2,2-trifluoroethylcarbonyloxy orO—COC₂F₅;

(C₁-C₄-alkoxy)carbonyl: COOCH₃, COOC₂H₅, n-propoxycarbonyl, COOCH(CH₃)₂,n-butoxycarbonyl, 1-(methylpropoxy)carbonyl, 2-(methylpropoxy)carbonylor COOC(CH₃)₃, in particular COOCH₃, COOC₂H₅ or COOC(CH₃)₃;

(C₁-C₄-alkoxy)carbonyl-C₁-C₄-alkyl: C₁-C₄-alkyl which is substituted by(C₁-C₄-alkoxy)carbonyl as mentioned above, i.e. CH₂COOCH₃, CH₂COOC₂H₅,CH₂CH₂COOCH₃, CH₂CH₂COOC₂H₅, CH(CH₃)COOCH₃ or CH(CH₃)COOC₂H₅;

(C₁-C₄-halogenalkoxy)carbonyl-C₁-C₄-alkyl:(C₁-C₄-alkoxy)carbonyl-C₁-C₄-alkyl as mentioned above whose alkoxymoiety is partially or fully substituted by fluorine, chlorine, bromineand/or iodine, i.e. CH₂COOCH₂CF₃ or CH(CH₃)COOCH₂CF₃;

(C₁-C₄-alkylthio)carbonyl-C₁-C₄-alkyl: C₁-C₄-alkyl which is substitutedby (C₁-C₄-alkylthio)carbonyl such as COSCH₃, COSC₂H₅,n-propylthiocarbonyl, 1-methylethylthiocarbonyl, n-butylthiocarbonyl,1-methylpropylthiocarbonyl, 2-methylpropylthiocarbonyl or1,1-dimethylethylthiocarbonyl, in particular COSCH₃ or COSC₂H₅, i.e.CH₂COSCH₃ or CH₂COSC₂H₅;

di(C₁-C₄-alkyl)amino and the dialkylamino moiety ofdi(C₁-C₄-alkyl)aminocarbonyl: for example N(CH₃)₂, N(C₂H₅)₂,N,N-dipropylamino, N,N-di-(1-methylethyl)amino, N,N-dibutylamino,N,N-di-(1-methylpropyl)amino, N,N-di-(2-methylpropyl)amino,N,N-di-(1,1-dimethylethyl)amino, N-ethyl-N-methylamino,N-methyl-N-propylamino, N-methyl-N-(1-methylethyl)amino,N-butyl-N-methylamino, N-methyl-N-(1-methylpropyl)amino,N-methyl-N-(2-methylpropyl)amino, N-(1,1-dimethylethyl)-N-methylamino,N-ethyl-N-propylamino, N-ethyl-N-(1-methylethyl)amino,N-butyl-N-ethylamino, N-ethyl-N-(1-methylpropyl)amino,N-ethyl-N-(2-methylpropyl)amino, N-ethyl-N-(1,1-dimethylethyl)amino,N-(1-methylethyl)-N-propylamino, N-butyl-N-propylamino,N-(1-methylpropyl)-N-propylamino, N-(2-methylpropyl)-N-propylamino,N-(1,1-dimethylethyl)-N-propylamino, N-butyl-N-(1-methylethyl)amino,N-(1-methylethyl)-N-(1-methylpropyl)amino,N-(1-methylethyl)-N-(2-methylpropyl)amino,N-(1,1-dimethylethyl)-N-(1-methylethyl)amino,N-butyl-N-(1-methylpropyl)amino, N-butyl-N-(2-methylpropyl)amino,N-butyl-N-(1,1-dimethylethyl)amino,N-(1-methylpropyl)-N-(2-methylpropyl)amino,N-(1,1-dimethylethyl)-N-(1-methylpropyl)amino orN-(1,1-dimethylethyl)-N-(2-methylpropyl)amino, in particular N(CH₃)₂ orN(C₂H₅)₂;

di(C₁-C₄-alkyl)amino-C₁-C₄-alkyl: C₁-C₄-alkyl which is substituted bydi(C₁-C₄-alkyl)amino as mentioned above, i.e. CH₂N(CH₃)₂, CH₂N(C₂H₅)₂,N,N-dipropylaminomethyl, N,N-di(1-methylethyl)aminomethyl,N,N-dibutylaminomethyl, N,N-di(1-methylpropyl)aminomethyl,N,N-di(2-methylpropyl)aminomethyl, N,N-di(1,1-dimethylethyl)aminomethyl,N-ethyl-N-methylaminomethyl, N-methyl-N-propylaminomethyl,N-methyl-N-(1-methylethyl)aminomethyl, N-butyl-N-methylaminomethyl,N-methyl-N-(1-methylpropyl)aminomethyl,N-methyl-N-(2-methylpropyl)aminomethyl,N-(1,1-dimethylethyl)-N-methylaminomethyl, N-ethyl-N-propylaminomethyl,N-ethyl-N-(1-methylethyl)aminomethyl, N-butyl-N-ethylaminomethyl,N-ethyl-N-(1-methylpropyl)aminomethyl,N-ethyl-N-(2-methylpropyl)aminomethyl,N-ethyl-N-(1,1-dimethylethyl)aminomethyl,N-(1-methylethyl)-N-propylaminomethyl, N-butyl-N-propylaminomethyl,N-(1-methylpropyl)-N-propylaminomethyl,N-(2-methylpropyl)-N-propylaminomethyl,N-(1,1-dimethylethyl)-N-propylaminomethyl,N-butyl-N-(1-methylethyl)aminomethyl,N-(1-methylethyl)-N-(1-methylpropyl)aminomethyl,N-(1-methylethyl)-N-(2-methylpropyl)aminomethyl,N-(1,1-dimethylethyl)-N-(1-methylethyl)aminomethyl,N-butyl-N-(1-methylpropyl)aminomethyl,N-butyl-N-(2-methylpropyl)aminomethyl,N-butyl-N-(1,1-dimethylethyl)aminomethyl,N-(1-methylpropyl)-N-(2-methylpropyl)aminomethyl,N-(1,1-dimethylethyl)-N-(1-methylpropyl)aminomethyl,N-(1,1-dimethylethyl)-N-(2-methylpropyl)aminomethyl,N,N-dimethylaminoethyl, N,N-diethylaminoethyl,N,N-di(n-propyl)aminoethyl, N,N-di(1-methylethyl)aminoethyl,N,N-dibutylaminoethyl, N,N-di(1-methylpropyl)aminoethyl,N,N-di(2-methylpropyl)aminoethyl, N,N-di(1,1-dimethylethyl)aminoethyl,N-ethyl-N-methylaminoethyl, N-methyl-N-propylaminoethyl,N-methyl-N-(1-methylethyl)aminoethyl, N-butyl-N-methylaminoethyl,N-methyl-N-(1-methylpropyl)aminoethyl,N-methyl-N-(2-methylpropyl)aminoethyl,N-(1,1-dimethylethyl)-N-methylaminoethyl, N-ethyl-N-propylaminoethyl,N-ethyl-N-(1-methyl-ethyl)aminoethyl, N-butyl-N-ethylaminoethyl,N-ethyl-N-(1-methylpropyl)aminoethyl,N-ethyl-N-(2-methylpropyl)aminoethyl,N-ethyl-N-(1,1-dimethylethyl)aminoethyl,N-(1-methylethyl)-N-propylaminoethyl, N-butyl-N-propylaminoethyl,N-(1-methylpropyl)-N-propylaminoethyl,N-(2-methylpropyl)-N-propylaminoethyl,N-(1,1-dimethylethyl)-N-propylaminoethyl,N-butyl-N-(1-methylethyl)aminoethyl,N-(1-methylethyl)-N-(1-methylpropyl)aminoethyl,N-(1-methylethyl)-N-(2-methylpropyl)aminoethyl,N-(1,1-dimethylethyl)-N-(1-methylethyl)aminoethyl,N-butyl-N-(1-methylpropyl)aminoethyl,N-butyl-N-(2-methylpropyl)aminoethyl,N-butyl-N-(1,1-dimethylethyl)aminoethyl,N-(1-methylpropyl)-N-(2-methylpropyl)aminoethyl,N-(1,1-dimethylethyl)-N-(1-methylpropyl)aminoethyl orN-(1,1-dimethylethyl)-N-(2-methylpropyl)aminoethyl, in particularN,N-dimethylaminoethyl or N,N-diethylaminoethyl;

di(C₁-C₄-alkyl)aminocarbonyl: a di(C₁-C₄-alkyl)amino radical asmentioned above which is bonded via a carbonyl bridge, i.e. CON(CH₃)₂,CON(C₂H₅)₂, N,N-dipropylaminocarbonyl,N,N-di-(1-methylethyl)aminocarbonyl, N,N-dibutylaminocarbonyl,N,N-di-(1-methylpropyl)aminocarbonyl,N,N-di-(2-methylpropyl)aminocarbonyl,N,N-di-(1,1-dimethylethyl)aminocarbonyl, N-ethyl-N-methylaminocarbonyl,N-methyl-N-propylaminocarbonyl, N-methyl-N-(1-methylethyl)aminocarbonyl,N-butyl-N-methylaminocarbonyl, N-methyl-N-(1-methylpropyl)aminocarbonyl,N-methyl-N-(2-methylpropyl)aminocarbonyl,N-(1,1-dimethylethyl)-N-methylaminocarbonyl,N-ethyl-N-propylaminocarbonyl, N-ethyl-N-(1-methylethyl)aminocarbonyl,N-butyl-N-ethylaminocarbonyl, N-ethyl-N-(1-methylpropyl)aminocarbonyl,N-ethyl-N-(2-methylpropyl)aminocarbonyl,N-ethyl-N-(1,1-dimethylethyl)aminocarbonyl,N-(1-methylethyl)-N-propylaminocarbonyl, N-butyl-N-propylaminocarbonyl,N-(1-methylpropyl)-N-propylaminocarbonyl,N-(2-methylpropyl)-N-propylaminocarbonyl,N-(1,1-dimethylethyl)-N-propylaminocarbonyl,N-butyl-N-(1-methylethyl)aminocarbonyl,N-(1-methylethyl)-N-(1-methylpropyl)aminocarbonyl,N-(1-methylethyl)-N-(2-methylpropyl)aminocarbonyl,N-(1,1-dimethylethyl)-N-(1-methylethyl)aminocarbonyl,N-butyl-N-(1-methylpropyl)aminocarbonyl,N-butyl-N-(2-methylpropyl)aminocarbonyl,N-butyl-N-(1,1-dimethylethyl)aminocarbonyl,N-(1-methylpropyl)-N-(2-methylpropyl)aminocarbonyl,N-(1,1-dimethylethyl)-N-(1-methylpropyl)aminocarbonyl, orN-(1,1-dimethylethyl)-N-(2-methylpropyl)aminocarbonyl;

di(C₁-C₄-alkyl)aminocarbonyl-C₁-C₄-alkyl: C₁-C₄-alkyl which issubstituted by di(C₁-C₄-alkyl)aminocarbonyl as mentioned above, i.e.CH₂—CON(CH₃)₂, CH₂—CON(C₂H₅)₂, N,N-dipropylamino-COCH₂-,N,N-di-(1-methylethyl)amino-COCH₂-, N,N-dibutylamino-COCH₂-,N,N-di-(1-methylpropyl)amino-COCH₂-, N,N-di(2-methylpropyl)amino-COCH₂-,N,N-di-(1,1-dimethylethyl)amino-COCH₂-, N-ethyl-N-methylamino-COCH₂-,N-methyl-N-propylamino-COCH₂-, N-methyl-N-(1-methylethyl)amino-COCH₂-,N-butyl-N-methylamino-COCH₂-, N-methyl-N-(1-methylpropyl)amino-COCH₂-,N-methyl-N-(2-methylpropyl)amino-COCH₂-,N-(1,1-dimethylethyl)-N-methylamino-COCH₂-,N-ethyl-N-propylamino-COCH₂-, N-ethyl-N-(1-methylethyl)amino-COCH₂-,N-butyl-N-ethylamino-COCH₂-, N-ethyl-N-(1-methylpropyl)amino-COCH₂-,N-ethyl-N-(2-methylpropyl)amino-COCH₂-,N-ethyl-N-(1,1-dimethylethyl)amino-COCH₂-,N-(1-methylethyl)-N-propylamino-COCH₂-, N-butyl-N-propylamino-COCH₂-,N-(1-methylpropyl)-N-propylamino-COCH₂-,N-(2-methylpropyl)-N-propylamino-COCH₂-,N-(1,1-dimethylethyl)-N-propylamino-COCH₂-,N-butyl-N-(1-methylethyl)amino-COCH₂-,N-(1-methylethyl)-N-(1-methylpropyl)amino-COCH₂-,N-(1-methylethyl)-N-(2-methylpropyl)amino-COCH₂-,N-(1,1-dimethylethyl)-N-(1-methylethyl)amino-COCH₂-,N-butyl-N-(1-methylpropyl)amino-COCH₂-,N-butyl-N-(2-methylpropyl)amino-COCH₂-,N-butyl-N-(1,1-dimethylethyl)amino-COCH₂-,N-(1-methylpropyl)-N-(2-methylpropyl)amino-COCH₂-,N-(1,1-dimethylethyl)-N-(1-methylpropyl)amino-COCH₂-,N-(1,1-dimethylethyl)-N-(2-methylpropyl)amino-COCH₂-, C₂H₄—CON(CH₃)₂,C₂H₄—CON(C₂H₅)₂, N,N-di(n-propyl)amino-COC₂H₄-,N,N-di-(1-methylethyl)amino-COC₂H₄-, N,N-dibutylamino-COC₂H₄-,N,N-di-(1-methylpropyl)amino-COC₂H₄-,N,N-di(2-methylpropyl)amino-COC₂H₄-,N,N-di(1,1-dimethylethyl)amino-COC₂H₄-, N-ethyl-N-methylamino-COC₂H₄-,N-methyl-N-propylamino-COC₂H₄-, N-methyl-N-(1-methylethyl)amino-COC₂H₄-,N-butyl-N-methylamino-COC₂H₄-, N-methyl-N-(1-methylpropyl)amino-COC₂H₄-,N-methyl-N-(2-methylpropyl)amino-COC₂H₄-,N-(1,1-dimethylethyl)-N-methylamino-COC₂H₄-,N-ethyl-N-propylamino-COC₂H₄-, N-ethyl-N-(1-methylethyl)amino-COC₂H₄-,N-butyl-N-ethylamino-COC₂H₄-, N-ethyl-N-(1-methylpropyl)amino-COC₂H₄-,N-ethyl-N-(2-methylpropyl)amino-COC₂H₄-,N-ethyl-N-(1,1-dimethylethyl)amino-COC₂H₄-,N-(1-methylethyl)-N-propylamino-COC₂H₄-, N-butyl-N-propylamino-COC₂H₄-,N-(1-methylpropyl)-N-propylamino-COC₂H₄-,N-(2-methylpropyl)-N-propylamino-COC₂H₄-,N-(1,1-dimethylethyl)-N-propylamino-COC₂H₄-,N-Butyl-N-(1-methylethyl)amino-COC₂H₄-,N-(1-methylethyl)-N-(1-methylpropyl)amino-COC₂H₄-,N-(1-methylethyl)-N-(2-methylpropyl)amino-COC₂H₄-,N-(1,1-dimethylethyl)-N-(1-methylethyl)amino-COC₂H₄-,N-butyl-N-(1-methylpropyl)amino-COC₂H₄-,N-butyl-N-(2-methylpropyl)amino-COC₂H₄-,N-butyl-N-(1,1-dimethylethyl)amino-COC₂H₄-,N-(1-methylpropyl)-N-(2-methylpropyl)amino-COC₂H₄-,N-(1,1-dimethylethyl)-N-(1-methylpropyl)amino-COC₂H₄- orN-(1,1-dimethylethyl)-N-(2-methylpropyl)amino-COC₂H₅-, in particularCH₂—CON(CH₃)₂, CH₂—CON(C₂H₅)₂, CH(CH₃)—CON(CH₃)₂ or CH(CH₃)CON(C₂H₅)₂;

C₁-C₄-alkyamino-C₁-C₄-alkyl: C₁-C₄-alkyl which is substituted byC₁-C₄-alkylamino, such as H₃C—NH—, H₅C₂—NH—, n-propyl-NH—,1-methylethyl-NH—, n-butyl-NH—, 1-methylpropyl-NH—, (H₃C)₂CH—CH—CH₂—NH—and 1,1-dimethylethyl—NH—, preferably H₃C—NH— or H₂C₂—NH—, ie., forexample CH₂CH₂—NH—CH₃, CH₂CH₂—N(CH₃)₂, CH₂CH₂—NH—C₂H₅ orCH₂CH₂—N(C₂H₅)₂;

(C₁-C₄-alkylamino)carbonyl: H₃C—NH—CO—, H₅C₂—NH—CO—, n-propyl-NH—CO,1-methylethyl-NH—CO—, n-butyl—NH—CO—, 1-methylpropyl-NH-CO,—CONH—CH₂—(CH₃)₂ or —CONH—C(CH₃)₃, in particular —CONH—CH₃ or—CONH—C₂H₅;

(C₁-C₄-alkylamino)carbonyl-C₁-C₄-alkyl: C₁-C₄-alkyl which is substitutedby (C₁-C₄-alkyamino)carbonyl as mentioned above, ie., for example,CH₂—CONH—CH₃, CH₂—COHN—C₂H₅, CH(CH₃)—CONH—CH₃ or CH(CH₃)—CONH—C₂H₅;

C₃-C₆-alkenyl: prop-1-en-1-yl, prop-2-en-1-yl, 1-methylethenyl,n-buten-1-yl, n-buten-2-yl, n-buten-3-yl, 1-methyl-prop-1-en-1-yl,2-methylprop-2-en-1-yl, n-penten-1-yl, n-penten-2-yl, n-penten-3-yl,n-penten-4-yl, 1-methylbut-1-en-1-yl, 2-methylbut-1-en-1-yl,2-methylbut-2-en-1-yl, 3-methylbut-2-en-1-yl, 1-methylbut-3-en-1-yl,1,1-dimethylprop-2-en-1-yl, 1,2-dimethylprop-1-en-1-yl,1,2-dimethylprop-2-ene-1-yl, 1-ethylprop-1-en-2-yl,1-ethylprop-2-en-1-yl, n-hex-1-en-1-yl, n-hex-2-en-1-yl,n-hex-3-en-1-yl, n-hex-4-en-1-yl, n-hex-5-en-1-yl,1-methyl-pent-1-en-1-yl, 2-methylpent-1-en-1-yl, 3-methylpent-1-en-1-yl,4-methylpent-1-en-1-yl, 1-methylpent-2-en-1-yl, 2-methylpent-2-en-1-yl,3-methylpent-2-en-1-yl, 4-methyl-pent-2-en-1-yl, 1-methylpent-3-en-1-yl,2-methylpent-3-en-1-yl, 3-methylpent-3-en-1-yl, 4-methylpent-3-en-1-yl,1-methylpent-4-en-1-yl, 2-methylpent-4-en-1-yl, 3-methylpent-4-en-1-yl,4-methylpent-4-en-1-yl, 1,1-dimethyl-but-2-en-1-yl,1,1-dimethylbut-3-en-1-yl, 1,2-dimethylbut-1-en-1-yl,1,2-dimethylbut-2-en-1-yl, 1,2-dimethylbut-3-en-1-yl,1,3-dimethylbut-1-en-1-yl, 1,3-dimethylbut-2-en-1-yl,1,3-dimethylbut-3-en-1-yl, 2,2-dimethylbut-3-en-1-yl,2,3-dimethylbut-1-en-1-yl, 2,3-dimethylbut-2-en-1-yl,2,3-dimethylbut-3-en-1-yl, 3,3-dimethylbut-1-en-1-yl,3,3-dimethyl-but-2-en-1-yl, 1-ethylbut-1-en-1-yl, 1-ethylbut-2-en-1-yl,1-ethylbut-3-en-1-yl, 2-ethylbut-1-en-1-yl, 2-ethylbut-2-en-1-yl,2-ethylbut-3-en-1-yl, 1,2,3-trimethylprop-2-en-1-yl,1-ethyl-1-methylprop-2-en-1-yl, 1-ethyl-2-methylprop-1-en-1-yl or1-ethyl-2-methylprop-2-en-1-yl, in particular allyl or 2-buten-1-yl;

C₃-C₆-haloalkenyl; C₃-C₆-alkenyl as mentioned above which is partiallyor fully substituted by fluorine, chlorine, bromine and/or iodine, ie.,for example, 2-chloroallyl, 3-chloroallyl, 2,3-dichloroallyl,3,3-dichloroallyl, 2,3,3-trichloroallyl, 2,3-dichlorobut-2-enyl,2-bromoallyl, 3-bromoallyl, 2,3-dibromoallyl, 3,3-dibromoallyl,2,3,3-tribromoallyl or 2,3-dibromobut-2-enyl, in particular2-chloroallyl, 3-chloroallyl or 3,3-dichloroallyl;

cyano-C₃-C₆-alkenyl; for example 2-cyanoallyl, 3-cyanoallyl,4-cyanobut-2-enyl, 4-cyanobut-3-enyl or 5-cyanopent-4-enyl, inparticular 3-cyanoallyl or 4-cyanobut-2-enyl;

C₃-C₆-alkynyl: prop-1-yl, propargyl, n-but-1-yn-1-yl, n-but-1-yn-3-yl,n-but-1-yn-4-yl, n-but-2-yn-1-yl, n-pent-1-yn-1-yl, n-pent-1-yn-3-yl,n-pent-1-yn-4-yl, n-pent-1-yn-5-yl, n-pent-2-yn-1-yl; n-pent-2-yn-4-yl,n-pent-2-yn-5-yl, 3-methylbut-1-yn-3-yl, 3-methylbut-1-yn-4-yl,n-hex-1-yn-1-yl, n-hex-1-yn-3-yl, n-hex-1-yn-4-yl, n-hex-1-yn-5-yl,n-hex-1-yn-6-yl, n-hex-2-yn-1-yl, n-hex-2-yn-4-yl, n-hex-2-yn-5-yl,n-hex-2-yn-6-yl, n-hex-3-yn-1-yl, n-hex-3-yn-2-yl,3-methylpent-1-yn-1-yl, 3-methylpent-1-yn-3-yl, 3-methylpent-1-yn-4-yl,3-methylpent-1-yn-5-yl, 4-methylpent-1-yn-1-yn, 4-methylpent-2-yn-4-ylor 4-methylpent-2-yn-5-yl, in particular propargyl;

C₃-C₆-haloalkyl: C₃-C₆-alkynyl as mentioned above which is partially orfully substituted by fluorine, chlorine, bromine and/or iodine, ie., forexample, 1,1-difluoroprop-2-yn-1-yl, 4-fluorobut-2-yn-1-yl,4-chlorobut-2-yn-1-yl, 1,1-difluorobut-2-yn-1-yl, 5-fluoropent-3-yn-1-ylor 6-fluoro-hex-4-yn-1-yl, in particular 4-fluorobut-2-yn-1-yl;

cyano-C₃-C₆-alkynl; for example 3-cyanopropargyl, 4-cyano-but-2-yn-1-yl,5-cyanopent-3-yn-1-yl and 6-cyanohex-4-yn-1-yl;

C₃-C₄-alkenyloxy-C₁-C₄-alkyl: C₁-C₄-alkyl which is substituted byC₃-C₄-alkenyloxy, such as allyloxy, but 1-en-3-yloxy, but-1-en-4-yloxy,but-2-en-1-yloxy, 1-methylprop-2-enyloxy or 2-methylprop-2-enyloxy, ie.,for example allyloxymethyl, 2-allyloxyethyl or but-1-en-4-yloxymethyl,in particular 2-allyloxyethyl;

C₃-C₄-alkynyloxy-C₁-C₄-alkyl which is substituted by C₃-C₄-alkynyloxy,such as propargyloxy, but-1-yn-3-yloxy, but-1-yn-4-yloxy,but-2-yn-1-yloxy, 1-methylprop-1-ynyloxy or 2-methylprop-2-ynloxy,preferably propargyloxy, ie., for example, propargyloxymethyl or2-propargyloxyethy, in particular 2-propargyloxyethyl;

(C₃-C₄-alkenyloxy)imino-C₁-C₄-alkyl; C₁-C₄-alkyl which is substituted by(C₃-C₄-alkenyloxy)imino, such as allyloxy, but-1-en-3-yloxyimino,but-1-en-4-yloxyimino, but-2-en-1-yloxyimino,1-methylprop-2-enyloxyimino or 2-methylprop-2-enyloxyimino, ie., forexample, allyloxyiminomethyl, 2-(allyloxyimino)ethyl orbut-1-en-4-yloxyiminomethyl, in particular 2-(allyoxyimino)ethyl or2-(2-buten-1-yloxyimino)ethyl;

C₃-C₄-alkenylthio-C₁-C₄-alkyl; C₁-C₄-alkyl which is substituted byC₃-C₄-alkenylthio, such as allyththio, but-1-en-3-yl-thio,but-1-en-4-ylthio, but-2-en-1-ylthio, 1-methylprop-2-enylthio or2-methylprop-2-enylthio, ie., for example, allylthiomethyl,2-allylthioethyl or but-1-en-4-ylthiomethyl, in particular2-(allylthio)ethyl;

C₃-C₄-alkenylthio-C₁-C₄-alkyl; C₁-C₄-alkyl which is substituted byC₃-C₄-alkenylthio, such as propargylthio, but-1-yn-3-ylthio,but-1-yn-4-ylthio, but-2-yn-1-ylthio, 1-methylprop-2-ynylthio or2-methylprop-2-ynylthio, preferably propargylthio, ie., for example,propargylthiomethyl or 2-propargylthioethyl, in particular2-(propargylthio)ethyl;

C₃-C₄-alkenylthio-C₁-C₄-alkyl; C₁-C₄-alkyl which is substituted byC₃-C₄-alkenylthio, such as allysulfinyl, but-1-en-3-ylsulfinyl,but-1-en-4-ylsulfinyl, but-2-en-1-yl-sulfinyl,1-methylprop-2-enylsulfinyl or 2-methylprop-2-enyl-sulfinyl, ie., forexample, allylsulfinylmethyl, 2-allysulfinylethyl orbut-1-en-4-ylsulfinylmethyl, in particular 2-(allylsulfinyl)ethyl;

C₃-C₄-alkenylthio-C₁-C₄-alkyl; C₁-C₄-alkyl which is substituted byC₃-C₄-alkenylthio, such as propargylsulfinyl, but-1-en-3-ylsulfinyfl,but-1-yn-4-ylsulfinyl, but-2-yn-1-yl-sulfinyl,1-methylprop-2-ynylsulfinyl or 2-methylprop-2-ynyl-sulfinyl, preferablypropargylsulfinyl, ie., for example, propargylsulfinylfmethyl or2-proparglysulfinylethyl, in particular 2-(propargylsulfinyl)ethyl;

C₃-C₄-alkenylthio-C₁-C₄-alkyl; C₁-C₄-alkyl which is substituted byC₃-C₄-alkenylthio, such as allylsulfonyl, but-1-en-3-sulfonyl,but-1-en-4-ylsulfonyl, but-2-en-1-yl-sulfonyl,1-methylprop-2-enylsulfonyl or 2-methylprop-2-enyl-sulfonyl, ie., forexample, allylsulfonylmethyl, 2-allysulfonylethyl orbut-1-en-4-ylsulfonylmethyl, in particular 2-(allysulfonyl)ethyl;

C₃-C₄-alkenylthio-C₁-C₄-alkyl; C₁-C₄-alkyl which is substituted byC₃-C₄-alkenylthio, such as propargylsulfonyl, but-1-yn-3-ylsulfonyl,but-1-yn-4-ylsulfony, but-2-yn-1-yl-sulfonyl,1-methylprop-2-ynylsulfonyl or 2-methylprop-2-ynyl-sulfonyl, preferablypropargylsulfonyl, ie., for example, propargylsulfonylmethyl or2-propargylsulfonylethyl, in particular 2-(propargylsulfonyl)ethyl.

3- to 7-membered heterocycle is to be understood as meaning saturated,partially or fully unsaturated and also aromatic heterocycles having oneto three hetero atoms selected from a group consisting of:

one to three nitrogen atoms,

one or two oxygen atoms and

one or two sulfur atoms.

Examples of saturated heterocycles which can contain a carbonyl orthiocarbonyl ring member are:

oxiranyl, thiiranyl, aziridin-1-yl, aziridin-2-yl, diaziridin-1-yl,diaziridin-3-yl, oxetan-2-yl, oxetan-3-yl, thietan-2-yl, thietan-3-yl,azetidin-1-yl, azetidin-2-yl, azetidin-3-yl, tetra-hydrofuran-2-yl,tetrahydrofuran-3-yl, tetrahydrothiophen-2-yl, tetrahydrothiophen-3-yl,pyrrolidin-1-yl, pyrrolidin-2-yl, pyrrolidin-3-yl, 1,3-dioxolan-2-yl,1,3-dioxolan-4-yl, 1,3-oxathiolan-2-yl, 1,3-oxathiolan-4-yl,1,3-oxathiolan-5-yl, 1,3-oxazolidin-2-yl, 1,3-oxazolidin-3-yl,1,3-oxazolidin-4-yl, 1,3-oxazolidin-5-yl, 1,2-oxazolidin-2-yl,1,2-oxazolidin-3-yl, 1,2-oxazolidin-4-yl, 1,2-oxazolidin-5-yl,1,3-dithiolan-2-yl, 1,3-dithiolan-4-yl, pyrrolidin-1-yl,pyrrolidin-2-yl, pyrrolidin-5-yl, tetrahydropyrazol-1-yl,tetrahydropyrazol-3-yl, tetrahydropyrazol-4-yl, tetrahydropyran-2-yl,tetrahydropyran-3-yl, tetrahydropyran-4-yl, tetrahydrothiopyran-2-yl,tetrahydrothiopyran-3-yl, tetrahydropyran-4-yl, piperidin-1-yl,piperidin-2-yl, piperidin-3-yl, piperidin-4-yl, 1,3-dioxan-2-yl,1,3-dioxan-4-yl, 1,3-dioxan-5-yl, 1,4-dioxan-2-yl, 1,3-oxathioan-2-yl,1,3-oxathian-4-yl, 1,3-oxathian-5-yl, 1,3-oxathian-6-yl,1,4-oxathian-2-yl, 1,4-oxathian-3-yl, morpholin-2-yl, morpholin-3-yl,morpholin-4-yl, hexahydropyridazin-1-yl, hexahydropyridazin-3-yl,hexahydropyridazin-4-yl, hexahydropyrmidin-1-yl,hexahydropyrimidin-2-yl, hexahydropyrimidin-4-yl,hexahydropyrimidin-3-yl, hexahydropyridazin-4-yl,hexahydropyrimidin-1-yl, hexahydropyrimidin-2-yl,hexahydropyrimidin-4-yl, hexahydropyrimidin-5-yl, piperazin-1-yl,piperazin-2-yl, piperazin-3-yl, hexahydro-1,3,5-triazin-1-yl,hexahydro-1,3,5-triazin-2-yl, oxapan-2-yl, oxepan-3-yl, oxepan-4-yl,thiepan-2-yl, thiepan-3-yl, thiepan-4-yl, 1,3-dioxepan-2-yl,1,3-dioxepan-4-yl, 1,3-dioxepan-5-yl, 1,3-dioxepan-6-yl,1,3-dithiepan-2-yl, 1,3-dithiepan-2-yl, 1,3-dithiepan-2-yl,1,3-dithiepan-2-yl, 1,4-dioxepan-2-yl, 1,4-dioxepen-7-yl,hexahydroazepin-1-yl, hexahydroazepin-2-yl, hexahydroazepin-3-yl,hexahydroazepin-4-yl, hexahydro-1,3-diazepin-4-yl,hexahydro-1,4-diazepin-1-yl and hexahydro-1,4-diazepin-2-yl

Examples of unsaturated heterocycles which can contain a carbonyl orthiocarbonyl ring member are:

dihydrofuran-2-yl, 1,2-oxazolin-3-yl, 1,2-oxazolin-5-yl,1,3-oxazolin-2-yl;

Preferred amongstthe heteroaromatics are the 5- and 6-memberedstructures, ie., for example, furyl, such as 2-furyl and 3-furyl,thienyl, such as 2-thienyl and 3-thienyl, pyrrolyl, such as 2-pyrrolyland 3-pyrrolyl, isoxazolyl, such as 3-isoxazolyl, 4-isoxazolyl and5-isoxazolyl, isothizolyl, such as 3-isothiazolyl, 4-isothiazolyl and5-isothiazolyl, pyrazolyl, such as 3-pyrazolyl, 4-pyrazolyl and5-pyrazolyl, oxazolyl, such as 2-thiazolyl, 4-thiazolyl and 5-thiazolyl,imidazolyl, such as 2-imidazolyl and 4-imidazolyl, oxadiazolyl, such as1,2,4-oxadiazol-3-yl, 1,2,4-oxadiazol-5-yl and 1,3,4-oxadiazol-2-yl,thiadiazolyl, such as 1,2,4-thiadiazol-3-yl, 1,2,4-thiadiazol-5-yl and1,3,4-thiadiazol-2-yl, triazoll, such as 1,2,4-triazol-1-yl,1,2,4-triazol-3-yl and 1,2,4-triazol-4-yl, pyridinyl, such as2-pyridinyl, 3-pyridinyl and 4-pyridinyl, pyridazinyl, such as3-pyridazinyl, and 4-pyridazinyl, pyrimidinyl, such as 2-pyrimidinyl,4-pyrimidinyl and 5-pyrimidinyl, and furthermore 2-pyrazinyl,1,3,5-triazin-2-yl and 1,2,4-yl and 1,2,4-traizin-3-yl, in particularpyridyl, pyrimidyl, furanyl and thienyl.

All cycloalkyl, phenyl and heterocyclic rings are preferablyunsubstituted or have a substituent attached to them.

Preferred with a view to the use of the substituted 3-phenylpyrazoles Ias herbicides are those compounds I in which the variables have thefollowing meanings, in each case alone or in combination:

R¹ is C₁-C₄-alkyl, in particular methyl:

R² is C₁-C₄-haloalkyl, C₁-C₄-haloalkoxy or C₁-C₄-alkylsulfonyl, inparticular trifluoromethyl, difluoromethoxy or methylsulfonyl;difluoromethoxy is especially preferred;

R³ is cyano or halogen, in particular chlorine, bromine or fluorine;chlorine is especially preferred;

R⁴ is hydrogen, fluorine or chlorine, in particular fluorine orchlorine;

R⁵ is cyano, halogen, or C₁-C₄-haloalkyl, in particular chlorine,bromine, or trifluoromethyl; chlorine is especially preferred;

R⁶ is C₁-C₆-alkyl, C₁-C₆-haloalkyl, cyano-C₁-C₄-alkyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-alkylthio-C₁-C₄-alkyl,C₁-C₄-alkylsulfonyl-C₁-C₄-alkyl, C₃-C₆-alkenyl, C₃-C₆-haloalkenyl,C₃-C₆-alkynyl, (C₁-C₄-alkyl)carbonyl, (C₁-C₄-haloalkyl) carbonyl,(C₁-C₄-alkoxy)carbonyl, di)C₁-C₄-alkyl)amino-carbonyl,(C₁-C₄-alkyl)carbonyl-C₁-C₄-alkyl, (C₃-C₈-cycloalkyl)carbonyl-C₁-C₄-alkyl, (C₁-C₄-alkoxy)imino-C₁-C₄-alkyl,hydroxycarbonyl-C₁-C₄-alkyl, (C₁-C₄-alkoxy)carbonyl-C₁-C₄-alkyl wich canhave attached to it a (C₁-C₄-alkoxy)imino group, ordi(C₁-C₄-alkyl)aminocarbonyl-C₁-C₄-alkyl, C₃-C₈-cycloalkyl,C₃-C₈-cycloalkyl-C₁-C₄-alkyl or phenyl-C₁-C₄-alkyl, in particularC₁-C₆-alkyl, C₁-C₄-alkoxy-C₁-C₄-alkyl, C₃-C₆-alkenyl, C₃-C₆-alkynyl,(C₁-C₄-alkyl)carbonyl, (C₁-C₄-alkoxy)carbonyl,di(C₁-C₄-alkyl)aminocarbonyl, (C₁-C₄-alkyl)carbonyl-C₁-C₄-alkyl,(C₃-C₈-cycloalkyl)carbonyl-C₁-C₄-alkyl, (C₁-C₄-alkoxy)imino-C₁-C₄-alkyl,hydroxycarbonyl-C₁-C₄-alkyl, (C₁-C₄-alkoxy)carbonyl-C₁-C₄-alkyl whichcan have attached to it a (C₁-C₄-alkoxy)imino group, or di(C₁-C₄-alkyl)aminocarbonyl-C₁-C₄-alkyl or phenyl-C₁-C₄-alkyl; especially preferredare C₁-C₄-alkyl, C₁-C₄-alkenyl, C₁-C₆-alkynyl, (C₁-C₄-alkyl)carbonyl,(C₁-C₄-alkoxy)carbonyl, di(C₁-C₄-alkyl)aminocarbonyl,(C₁-C₄-alkoxy)carbonyl-C₁-C₄-alkyl ordi(C₁-C₄-alkyl)alminocarbonyl-C₁-C₄-alkyl;

R⁷ is C₁-C₄-alkyl, C₃-C₆-alkenyl, C₃-C₆-alkynyl,(C₁-C₄-alkoxy)-carbonyl-C₁-C₄-alkyl,di(C₁-C₄-alkyl)aminocarbonyl-C₁-C₄-alkyl, C₃-C₈-cycloalkyl,C₃-C₈-cycloalkyl-C₁-C₄-alkyl, phenyl or phenyl-C₁-C₄-alkyl, inparticular C₁-C₄-alkyl, C₃-C₆-alkenyl, C₃-C₆-alkenyl,(C₁-C₄-alkoxy)carbonyl-C₁-C₄-alkyl or phenyl-C₁-C₄-alkyl.

X is a chemical bond, a 1,2-ethynediyl group or a group *—CH═C(R⁸)—which is bonded to the phenyl ring via the side characterized with anasterisk, where R⁸ is hydrogen, cyano, chlorine, bromine or methyl, inparticular chlorine; X is especially preferably a chemical bond; and

Y is oxygen.

Very especially preferred are the compounds Ia which are listed in Table1 below (=I where R¹=methyl, R²=difluoromethoxy, R³ and R⁵=chlorine,X=chemical bond and Y=oxygen):

TABLE 1 I

No. R⁴ R⁶ R⁷ Ia.1 H CH₃ CH₃ Ia.2 F CH₃ CH₃ Ia.3 Cl CH₃ CH₃ Ia.4 H C₂H₅CH₃ Ia.5 F C₂H₅ CH₃ Ia.6 Cl C₂H₅ CH₃ Ia.7 H n-C₃H₇ CH₃ Ia.8 F n-C₃H₇ CH₃Ia.9 Cl n-C₃H₇ CH₃ Ia.10 H CH(CH₃)₂ CH₃ Ia.11 F CH(CH₃)₂ CH₃ Ia.12 ClCH(CH₃)₂ CH₃ Ia.13 H n-C₄H₉ CH₃ Ia.14 F n-C₄H₉ CH₃ Ia.15 Cl n-C₄H₉ CH₃Ia.16 H s-C₄H₉ CH₃ Ia.17 F s-C₄H₉ CH₃ Ia.18 Cl s-C₄H₉ CH₃ Ia.19 HCH₂—CH(CH₃)₂ CH₃ Ia.20 F CH₂—CH(CH₃)₂ CH₃ Ia.21 Cl CH₂—CH(CH₃)₂ CH₃Ia.22 H C(CH₃)₃ CH₃ Ia.23 F C(CH₃)₃ CH₃ Ia.24 Cl C(CH₃)₃ CH₃ Ia.25 Hn-C₅H₁₁ CH₃ Ia.26 F n-C₅H₁₁ CH₃ Ia.27 Cl n-C₅H₁₁ CH₃ Ia.28 H n-C₆H₁₃ CH₃Ia.29 F n-C₆H₁₃ CH₃ Ia.30 Cl n-C₆H₁₃ CH₃ Ia.31 H CH₃ C₂H₅ Ia.32 F CH₃C₂H₅ Ia.33 Cl CH₃ C₂H₅ Ia.34 H C₂H₅ C₂H₅ Ia.35 F C₂H₅ C₂H₅ Ia.36 Cl C₂H₅C₂H₅ Ia.37 H n-C₃H₇ C₂H₅ Ia.38 F n-C₃H₇ C₂H₅ Ia.39 Cl n-C₃H₇ C₂H₅ Ia.40H CH(CH₃)₂ C₂H₅ Ia.41 F CH(CH₃)₂ C₂H₅ Ia.42 Cl CH(CH₃)₂ C₂H₅ Ia.43 Hn-C₄H₉ C₂H₅ Ia.44 F n-C₄H₉ C₂H₅ Ia.45 Cl n-C₄H₉ C₂H₅ Ia.46 H s-C₄H₉ C₂H₅Ia.47 F s-C₄H₉ C₂H₅ Ia.48 Cl s-C₄H₉ C₂H₅ Ia.49 H CH₂—CH(CH₃)₂ C₂H₅ Ia.50F CH₂—CH(CH₃)₂ C₂H₅ Ia.51 Cl CH₂—CH(CH₃)₂ C₂H₅ Ia.52 H C(CH₃)₃ C₂H₅Ia.53 F C(CH₃)₃ C₂H₅ Ia.54 Cl C(CH₃)₃ C₂H₅ Ia.55 H n-C₅H₁₁ C₂H₅ Ia.56 Fn-C₅H₁₁ C₂H₅ Ia.57 Cl n-C₅H₁₁ C₂H₅ Ia.58 H n-C₆H₁₃ C₂H₅ Ia.59 F n-C₆H₁₃C₂H₅ Ia.60 Cl n-C₆H₁₃ C₂H₅ Ia.61 H CH₃ n-C₃H₇ Ia.62 F CH₃ n-C₃H₇ Ia.63Cl CH₃ n-C₃H₇ Ia.64 H C₂H₅ n-C₃H₇ Ia.65 F C₂H₅ n-C₃H₇ Ia.66 Cl C₂H₅n-C₃H₇ Ia.67 H n-C₃H₇ n-C₃H₇ Ia.68 F n-C₃H₇ n-C₃H₇ Ia.69 Cl n-C₃H₇n-C₃H₇ Ia.70 H CH(CH₃)₂ n-C₃H₇ Ia.71 F CH(CH₃)₂ n-C₃H₇ Ia.72 Cl CH(CH₃)₂n-C₃H₇ Ia.73 H n-C₄H₉ n-C₃H₇ Ia.74 F n-C₄H₉ n-C₃H₇ Ia.75 Cl n-C₄H₉n-C₃H₇ Ia.76 H s-C₄H₉ n-C₃H₇ Ia.77 F s-C₄H₉ n-C₃H₇ Ia.78 Cl s-C₄H₉n-C₃H₇ Ia.79 H CH₂—CH(CH₃)₂ n-C₃H₇ Ia.80 F CH₂—CH(CH₃)₂ n-C₃H₇ Ia.81 ClCH₂—CH(CH₃)₂ n-C₃H₇ Ia.82 H C(CH₃)₃ n-C₃H₇ Ia.83 F C(CH₃)₃ n-C₃H₇ Ia.84Cl C(CH₃)₃ n-C₃H₇ Ia.85 H n-C₅H₁₁ n-C₃H₇ Ia.86 F n-C₅H₁₁ n-C₃H₇ Ia.87 Cln-C₅H₁₁ n-C₃H₇ Ia.88 H n-C₆H₁₃ n-C₃H₇ Ia.89 F n-C₆H₁₃ n-C₃H₇ Ia.90 Cln-C₆H₁₃ n-C₃H₇ Ia.91 H CH₃ CH(CH₃)₂ Ia.92 F CH₃ CH(CH₃)₂ Ia.93 Cl CH₃CH(CH₃)₂ la.94 H C₂H₅ CH(CH₃)₂ Ia.95 F C₂H₅ CH(CH₃)₂ Ia.96 Cl C₂H₅CH(CH₃)₂ Ia.97 H n-C₃H₇ CH(CH₃)₂ Ia.98 F n-C₃H₇ CH(CH₃)₂ Ia.99 Cl n-C₃H₇CH(CH₃)₂ Ia.100 H CH(CH₃)₂ CH(CH₃)₂ Ia.101 F CH(CH₃)₂ CH(CH₃)₂ Ia.102 ClCH(CH₃)₂ CH(CH₃)₂ Ia.103 H n-C₄H₉ CH(CH₃)₂ Ia.104 F n-C₄H₉ CH(CH₃)₂Ia.105 Cl n-C₄H₉ CH(CH₃)₂ Ia.106 H s-C₄H₉ CH(CH₃)₂ Ia.107 F s-C₄H₉CH(CH₃)₂ Ia.108 Cl s-C₄H₉ CH(CH₃)₂ Ia.109 H CH₂—CH(CH₃)₂ CH(CH₃)₂ Ia.110F CH₂—CH(CH₃)₂ CH(CH₃)₂ Ia.111 Cl CH₂—CH(CH₃)₂ CH(CH₃)₂ Ia.112 H C(CH₃)₃CH(CH₃)₂ Ia.113 F C(CH₃)₃ CH(CH₃)₂ Ia.114 Cl C(CH₃)₃ CH(CH₃)₂ Ia.115 Hn-C₅H₁₁ CH(CH₃)₂ Ia.116 F n-C₅H₁₁ CH(CH₃)₂ Ia.117 Cl n-C₅H₁₁ CH(CH₃)₂Ia.118 H n-C₆H₁₃ CH(CH₃)₂ Ia.119 F n-C₆H₁₃ CH(CH₃)₂ Ia.120 Cl n-C₆H₁₃CH(CH₃)₂ Ia.121 H CH₃ n-C₄H₉ Ia.122 F CH₃ n-C₄H₉ Ia.123 Cl CH₃ n-C₄H₉Ia.124 H C₂H₅ n-C₄H₉ Ia.125 F C₂H₅ n-C₄H₉ Ia.126 Cl C₂H₅ n-C₄H₉ Ia.127 Hn-C₃H₇ n-C₄H₉ Ia.128 F n-C₃H₇ n-C₄H₉ Ia.129 Cl n-C₃H₇ n-C₄H₉ Ia.130 HCH(CH₃)₂ n-C₄H₉ Ia.131 F CH(CH₃)₂ n-C₄H₉ Ia.132 Cl CH(CH₃)₂ n-C₄H₉Ia.133 H n-C₄H₉ n-C₄H₉ Ia.134 F n-C₄H₉ n-C₄H₉ Ia.135 Cl n-C₄H₉ n-C₄H₉Ia.136 H s-C₄H₉ n-C₄H₉ Ia.137 F s-C₄H₉ n-C₄H₉ Ia.138 Cl s-C₄H₉ n-C₄H₉Ia.139 H CH₂—CH(CH₃)₂ n-C₄H₉ Ia.140 F CH₂—CH(CH₃)₂ n-C₄H₉ Ia.141 ClCH₂—CH(CH₃)₂ n-C₄H₉ Ia.142 H C(CH₃)₃ n-C₄H₉ Ia.143 F C(CH₃)₃ n-C₄H₉Ia.144 Cl C(CH₃)₃ n-C₄H₉ Ia.145 H n-C₅H₁₁ n-C₄H₉ Ia.146 F n-C₅H₁₁ n-C₄H₉Ia.147 Cl n-C₅H₁₁ n-C₄H₉ Ia.148 H n-C₆H₁₃ n-C₄H₉ Ia.149 F n-C₆H₁₃ n-C₄H₉Ia.150 Cl n-C₆H₁₃ n-C₄H₉ Ia.151 H CH₃ s-C₄H₉ Ia.152 F CH₃ s-C₄H₉ Ia.153Cl CH₃ s-C₄H₉ Ia.154 H C₂H₅ s-C₄H₉ Ia.155 F C₂H₅ s-C₄H₉ Ia.156 Cl C₂H₅s-C₄H₉ Ia.157 H n-C₃H₇ s-C₄H₉ Ia.158 F n-C₃H₇ s-C₄H₉ Ia.159 Cl n-C₃H₇s-C₄H₉ Ia.160 H CH(CH₃)₂ s-C₄H₉ Ia.161 F CH(CH₃)₂ s-C₄H₉ Ia.162 CiCH(CH₃)₂ s-C₄H₉ Ia.163 H n-C₄H₉ s-C₄H₉ Ia.164 F n-C₄H₉ s-C₄H₉ Ia.165 Cln-C₄H₉ s-C₄H₉ Ia.166 H s-C₄H₉ s-C₄H₉ Ia.167 F s-C₄H₉ s-C₄H₉ Ia.168 Cls-C₄H₉ s-C₄H₉ Ia.169 H CH₂—CH(CH₃)₂ s-C₄H₉ Ia.170 F CH₂—CH(CH₃)₂ s-C₄H₉Ia.171 Cl CH₂—CH(CH₃)₂ s-C₄H₉ Ia.172 H C(CH₃)₃ s-C₄H₉ Ia.173 F C(CH₃)₃s-C₄H₉ la.174 Cl C(CH₃)₃ s-C₄H₉ Ia.175 H n-C₅H₁₁ s-C₄H₉ Ia.176 F n-C₅H₁₁s-C₄H₉ Ia.177 Cl n-C₅H₁₁ s-C₄H₉ Ia.178 H n-C₆H₁₃ s-C₄H₉ Ia.179 F n-C₆H₁₃s-C₄H₉ Ia.180 Cl n-C₆H₁₃ s-C₄H₉ Ia.181 H CH₃ CH₂—CH(CH₃)₂ Ia.182 F CH₃CH₂—CH(CH₃)₂ Ia.183 Cl CH₃ CH₂—CH(CH₃)₂ Ia.184 H C₂H₅ CH₂—CH(CH₃)₂Ia.185 F C₂H₅ CH₂—CH(CH₃)₂ Ia.186 Cl C₂H₅ CH₂—CH(CH₃)₂ Ia.187 H n-C₃H₇CH₂—CH(CH₃)₂ Ia.188 F n-C₃H₇ CH₂—CH(CH₃)₂ Ia.189 Cl n-C₃H₇ CH₂—CH(CH₃)₂Ia.190 H CH(CH₃)₂ CH₂—CH(CH₃)₂ Ia.191 F CH(CH₃)₂ CH₂—CH(CH₃)₂ Ia.192 ClCH(CH₃)₂ CH₂—CH(CH₃)₂ Ia.193 H n-C₄H₉ CH₂—CH(CH₃)₂ Ia.194 F n-C₄H₉CH₂—CH(CH₃)₂ Ia.195 Cl n-C₄H₉ CH₂—CH(CH₃)₂ Ia.196 H s-C₄H₉ CH₂—CH(CH₃)₂Ia.197 F s-C₄H₉ CH₂—CH(CH₃)₂ Ia.198 Cl s-C₄H₉ CH₂—CH(CH₃)₂ Ia.199 HCH₂—CH(CH₃)₂ CH₂—CH(CH₃)₂ Ia.200 F CH₂—CH(CH₃)₂ CH₂—CH(CH₃)₂ Ia.201 ClCH₂—CH(CH₃)₂ CH₂—CH(CH₃)₂ Ia.202 H C(CH₃)₃ CH₂—CH(CH₃)₂ Ia.203 F C(CH₃)₃CH₂—CH(CH₃)₂ Ia.204 Cl C(CH₃)₃ CH₂—CH(CH₃)₂ Ia.205 H n-C₅H₁₁CH₂—CH(CH₃)₂ Ia.206 F n-C₅H₁₁ CH₂—CH(CH₃)₂ Ia.207 Cl n-C₅H₁₁CH₂—CH(CH₃)₂ Ia.208 H n-C₆H₁₃ CH₂—CH(CH₃)₂ Ia.209 F n-C₆H₁₃ CH₂—CH(CH₃)₂Ia.210 Cl n-C₆H₁₃ CH₂—CH(CH₃)₂ Ia.211 H CH₃ C(CH₃)₃ Ia.212 F CH₃ C(CH₃)₃Ia.213 Cl CH₃ C(CH₃)₃ Ia.214 H C₂H₅ C(CH₃)₃ Ia.215 F C₂H₅ C(CH₃)₃ Ia.216Cl C₂H₅ C(CH₃)₃ Ia.217 H n-C₃H₇ C(CH₃)₃ Ia.218 F n-C₃H₇ C(CH₃)₃ Ia.219Cl n-C₃H₇ C(CH₃)₃ Ia.220 H CH(CH₃)₂ C(CH₃)₃ Ia.221 F CH(CH₃)₂ C(CH₃)₃Ia.222 Cl CH(CH₃)₂ C(CH₃)₃ Ia.223 H n-C₄H₉ C(CH₃)₃ Ia.224 F n-C₄H₉C(CH₃)₃ Ia.225 Cl n-C₄H₉ C(CH₃)₃ Ia.226 H s-C₄H₉ C(CH₃)₃ Ia.227 F s-C₄H₉C(CH₃)₃ Ia.228 Cl s-C₄H₉ C(CH₃)₃ Ia.229 H CH₂—CH(CH₃)₂ C(CH₃)₃ Ia.230 FCH₂—CH(CH₃)₂ C(CH₃)₃ Ia.231 Cl CH₂—CH(CH₃)₂ C(CH₃)₃ Ia.232 H C(CH₃)₃C(CH₃)₃ Ia.233 F C(CH₃)₃ C(CH₃)₃ Ia.234 Cl C(CH₃)₃ C(CH₃)₃ Ia.235 Hn-C₅H₁₁ C(CH₃)₃ Ia.236 F n-C₅H₁₁ C(CH₃)₃ Ia.237 Cl n-C₅H₁₁ C(CH₃)₃Ia.238 H n-C₆H₁₃ C(CH₃)₃ Ia.239 F n-C₆H₁₃ C(CH₃)₃ Ia.240 Cl n-C₆H₁₃C(CH₃)₃ Ia.241 H CH₃ n-C₅H₁₁ Ia.242 F CH₃ n-C₅H₁₁ Ia.243 Cl CH₃ n-C₅H₁₁Ia.244 H C₂H₅ n-C₅H₁₁ Ia.245 F C₂H₅ n-C₅H₁₁ Ia.246 Cl C₂H₅ n-C₅H₁₁Ia.247 H n-C₃H₇ n-C₅H₁₁ Ia.248 F n-C₃H₇ n-C₅H₁₁ Ia.249 Cl n-C₃H₇ n-C₅H₁₁Ia.250 H CH(CH₃)₂ n-C₅H₁₁ Ia.251 F CH(CH₃)₂ n-C₅H₁₁ Ia.252 Cl CH(CH₃)₂n-C₅H₁₁ Ia.253 H n-C₄H₉ n-C₅H₁₁ Ia.254 F n-C₄H₉ n-C₅H₁₁ Ia.255 Cl n-C₄H₉n-C₅H₁₁ Ia.256 H s-C₄H₉ n-C₅H₁₁ Ia.257 F s-C₄H₉ n-C₅H₁₁ Ia.258 Cl s-C₄H₉n-C₅H₁₁ Ia.259 H CH₂—CH(CH₃)₂ n-C₅H₁₁ Ia.260 F CH₂—CH(CH₃)₂ n-C₅H₁₁Ia.261 Cl CH₂—CH(CH₃)₂ n-C₅H₁₁ Ia.262 H C(CH₃)₃ n-C₅H₁₁ Ia.263 F C(CH₃)₃n-C₅H₁₁ Ia.264 Cl C(CH₃)₃ n-C₅H₁₁ Ia.265 H n-C₅H₁₁ n-C₅H₁₁ Ia.266 Fn-C₅H₁₁ n-C₅H₁₁ Ia.267 Cl n-C₅H₁₁ n-C₅H₁₁ Ia.268 H n-C₆H₁₃ n-C₅H₁₁Ia.269 F n-C₆H₁₃ n-C₅H₁₁ Ia.270 Cl n-C₆H₁₃ n-C₅H₁₁ Ia.271 H CH₃ n-C₆H₁₃Ia.272 F CH₃ n-C₆H₁₃ Ia.273 Cl CH₃ n-C₆H₁₃ Ia.274 H C₂H₅ n-C₆H₁₃ Ia.275F C₂H₅ n-C₆H₁₃ Ia.276 Cl C₂H₅ n-C₆H₁₃ Ia.277 H n-C₃H₇ n-C₆H₁₃ Ia.278 Fn-C₃H₇ n-C₆H₁₃ Ia.279 Cl n-C₃H₇ n-C₆H₁₃ Ia.280 H CH(CH₃)₂ n-C₆H₁₃ Ia.281F CH(CH₃)₂ n-C₆H₁₃ Ia.282 Cl CH(CH₃)₂ n-C₆H₁₃ Ia.283 H n-C₄H₉ n-C₆H₁₃Ia.284 F n-C₄H₉ n-C₆H₁₃ Ia.285 Cl n-C₄H₉ n-C₆H₁₃ Ia.286 H s-C₄H₉ n-C₆H₁₃Ia.287 F s-C₄H₉ n-C₆H₁₃ Ia.288 Cl s-C₄H₉ n-C₆H₁₃ Ia.289 H CH₂—CH(CH₃)₂n-C₆H₁₃ la.290 F CH₂—CH(CH₃)₂ n-C₆H₁₃ Ia.291 Cl CH₂—CH(CH₃)₂ n-C₆H₁₃Ia.292 H C(CH₃)₃ n-C₆H₁₃ Ia.293 F C(CH₃)₃ n-C₆H₁₃ Ia.294 Cl C(CH₃)₃n-C₆H₁₃ Ia.295 H n-C₅H₁₁ n-C₆H₁₃ Ia.296 F n-C₅H₁₁ n-C₆H₁₃ Ia.297 Cln-C₅H₁₁ n-C₆H₁₃ Ia.298 H n-C₆H₁₃ n-C₆H₁₃ Ia.299 F n-C₆H₁₃ n-C₆H₁₃ Ia.300Cl n-C₆H₁₃ n-C₆H₁₃ Ia.301 H CH₂—CH₂—Cl CH₃ Ia.302 F CH₂—CH₂—Cl CH₃Ia.303 Cl CH₂—CH₂—Cl CH₃ Ia.304 H CH₂—CH₂—Cl C₂H₅ Ia.305 F CH₂—CH₂—ClC₂H₅ Ia.306 Cl CH₂—CH₂—Cl C₂H₅ Ia.307 H CH₂—CH₂—Cl n-C₃H₇ Ia.308 FCH₂—CH₂—Cl n-C₃H₇ Ia.309 Cl CH₂—CH₂—Cl n-C₃H₇ Ia.310 H CH₂—CH₂—Cl n-C₄H₉Ia.311 F CH₂—CH₂—Cl n-C₄H₉ Ia.312 Cl CH₂—CH₂—Cl n-C₄H₉ Ia.313 HCH₂—CH₂—Cl CH₂—CH═CH₂ Ia.314 F CH₂—CH₂—Cl CH₂—CH═CH₂ Ia.315 ClCH₂—CH₂—Cl CH₂—CH═CH₂ Ia.316 H CH₂—CH₂—Cl CH₂—C≡CH Ia.317 F CH₂—CH₂—ClCH₂—C≡CH Ia.318 Cl CH₂—CH₂—Cl CH₂—C≡CH Ia.319 H CH₂—CH₂—Cl CH₂—CO—OCH₃Ia.320 F CH₂—CH₂—Cl CH₂—CO—OCH₃ Ia.321 Cl CH₂—CH₂—Cl CH₂—CO—OCH₃ Ia.322H CH₂—CH₂—Cl CH₂-phenyl Ia.323 F CH₂—CH₂—Cl CH₂-phenyl Ia.324 ClCH₂—CH₂—Cl CH₂-phenyl Ia.325 H CH₂—CF₃ CH₃ Ia.326 F CH₂—CF₃ CH₃ Ia.327Cl CH₂—CF₃ CH₃ Ia.328 H CH₂—CF₃ C₂H₅ Ia.329 F CH₂—CF₃ C₂H₅ Ia.330 ClCH₂—CF₃ C₂H₅ Ia.331 H CH₂—CF₃ n-C₃H₇ Ia.332 F CH₂—CF₃ n-C₃H₇ Ia.333 ClCH₂—CF₃ n-C₃H₇ Ia.334 H CH₂—CF₃ n-C₄H₉ Ia.335 F CH₂—CF₃ n-C₄H₉ Ia.336 ClCH₂—CF₃ n-C₄H₉ Ia.337 H CH₂—CF₃ CH₂—CH═CH₂ Ia.338 F CH₂—CF₃ CH₂—CH═CH₂Ia.339 Cl CH₂—CF₃ CH₂—CH═CH₂ Ia.340 H CH₂—CF₃ CH₂—C≡CH Ia.341 F CH₂—CF₃CH₂—C≡CH Ia.342 Cl CH₂—CF₃ CH₂—C≡CH Ia.343 H CH₂—CF₃ CH₂—CO—OCH₃ Ia.344F CH₂—CF₃ CH₂—CO—OCH₃ Ia.345 Cl CH₂—CF₃ CH₂—CO—OCH₃ Ia.346 H CH₂—CF₃CH₂-phenyl Ia.347 F CH₂—CF₃ CH₂-phenyl Ia.348 Cl CH₂—CF₃ CH₂-phenylIa.349 H CH₂—CH₂—OH CH₃ Ia.350 F CH₂—CH₂—OH CH₃ Ia.351 Cl CH₂—CH₂—OH CH₃Ia.352 H CH₂—CH₂—OH C₂H₅ Ia.353 F CH₂—CH₂—OH C₂H₅ Ia.354 Cl CH₂—CH₂—OHC₂H₅ Ia.355 H CH₂—CH₂—OH n-C₃H₇ Ia.356 F CH₂—CH₂—OH n-C₃H₇ Ia.357 ClCH₂—CH₂—OH n-C₃H₇ Ia.358 H CH₂—CH₂—OH n-C₄H₉ Ia.359 F CH₂—CH₂—OH n-C₄H₉Ia.360 Cl CH₂—CH₂—OH n-C₄H₉ Ia.361 H CH₂—CH₂—OH CH₂—CH═CH₂ Ia.362 FCH₂—CH₂—OH CH₂—CH═CH₂ Ia.363 Cl CH₂—CH₂—OH CH₂—CH═CH₂ Ia.364 HCH₂—CH₂—OH CH₂—C≡CH Ia.365 F CH₂—CH₂—OH CH₂—C≡CH Ia.366 Cl CH₂—CH₂—OHCH₂—C≡CH Ia.367 H CH₂—CH₂—OH CH₂—CO—OCH₃ Ia.368 F CH₂—CH₂—OH CH₂—CO—OCH₃Ia.369 Cl CH₂—CH₂—OH CH₂—CO—OCH₃ Ia.370 H CH₂—CH₂—OH CH₂-phenyl Ia.371 FCH₂—CH₂—OH CH₂-phenyl Ia.372 Cl CH₂—CH₂—OH CH₂-phenyl Ia.373 HCH₂—CH(CH₃)—OH CH₃ Ia.374 F CH₂—CH(CH₃)—OH CH₃ Ia.375 Cl CH₂—CH(CH₃)—OHCH₃ Ia.376 H CH₂—CH(CH₃)—OH C₂H₅ Ia.377 F CH₂—CH(CH₃)—OH C₂H₅ Ia.378 CiCH₂—CH(CH₃)—OH C₂H₅ Ia.379 H CH₂—CH(CH₃)—OH n-C₃H₇ Ia.380 FCH₂—CH(CH₃)—OH n-C₃H₇ Ia.381 Cl CH₂—CH(CH₃)—OH n-C₃H₇ Ia.382 HCH₂—CH(CH₃)—OH n-C₄H₉ Ia.383 F CH₂—CH(CH₃)—OH n-C₄H₉ Ia.384 ClCH₂—CH(CH₃)—OH n-C₄H₉ Ia.385 H CH₂—CH(CH₃)—OH CH₂—CH═CH₂ Ia.386 FCH₂—CH(CH₃)—OH CH₂—CH═CH₂ Ia.387 Cl CH₂—CH(CH₃)—OH CH₂—CH═CH₂ Ia.388 HCH₂—CH(CH₃)—OH CH₂—C≡CH Ia.389 F CH₂—CH(CH₃)—OH CH₂—C≡CH Ia.390 ClCH₂—CH(CH₃)—OH CH₂—C≡CH Ia.391 H CH₂—CH(CH₃)—OH CH₂—CO—OCH₃ Ia.392 FCH₂—CH(CH₃)—OH CH₂—CO—OCH₃ Ia.393 Cl CH₂—CH(CH₃)—OH CH₂—CO—OCH₃ Ia.394 HCH₂—CH(CH₃)—OH CH₂-phenyl Ia.395 F CH₂—CH(CH₃)—OH CH₂-phenyl Ia.396 ClCH₂—CH(CH₃)—OH CH₂-phenyl Ia.397 H CH₂—CH₂—N CH₃ Ia.398 F CH₂—CH₂—N CH₃Ia.399 Cl CH₂—CH₂—N CH₃ Ia.400 H CH₂—CH₂—N C₂H₅ Ia.401 F CH₂—CH₂—N C₂H₅Ia.402 Cl CH₂—CH₂—N C₂H₅ Ia.403 H CH₂—CH₂—N n-C₃H₇ Ia.404 F CH₂—CH₂—Nn-C₃H₇ Ia.405 Cl CH₂—CH₂—N n-C₃H₇ Ia.406 H CH₂—CH₂—N n-C₄H₉ Ia.407 FCH₂—CH₂—N n-C₄H₉ Ia.408 Cl CH₂—CH₂—N n-C₄H₉ Ia.409 H CH₂—CH₂—NCH₂—CH═CH₂ Ia.410 F CH₂—CH₂—N CH₂—CH═CH₂ Ia.411 Cl CH₂—CH₂—CN CH₂—CH═CH₂Ia.412 H CH₂—CH₂—CN CH₂—C≡CH Ia.413 F CH₂—CH₂—CN CH₂—C≡CH Ia.414 ClCH₂—CH₂—CN CH₂—C≡CH Ia.415 H CH₂—CH₂—CN CH₂—CO—OCH₃ Ia.416 F CH₂—CH₂—CNCH₂—CO—OCH₃ Ia.417 Cl CH₂—CH₂—CN CH₂—CO—OCH₃ Ia.418 H CH₂—CH₂—CNCH₂-phenyl Ia.419 F CH₂—CH₂—CN CH₂-phenyl Ia.420 Cl CH₂—CH₂—CNCH₂-phenyl Ia.421 H CH₂—OCH₃ CH₃ Ia.422 F CH₂—OCH₃ CH₃ Ia.423 ClCH₂—OCH₃ CH₃ Ia.424 H CH₂—OCH₃ C₂H₅ Ia.425 F CH₂—OCH₃ C₂H₅ Ia.426 ClCH₂—OCH₃ C₂H₅ Ia.427 H CH₂—OCH₃ n-C₃H₇ Ia.428 F CH₂—OCH₃ n-C₃H₇ Ia.429Cl CH₂—OCH₃ n-C₃H₇ Ia.430 H CH₂—OCH₃ n-C₄H₉ Ia.431 F CH₂—OCH₃ n-C₄H₉Ia.432 Cl CH₂—OCH₃ n-C₄H₉ Ia.433 H CH₂—OCH₃ CH₂—CH═CH₂ Ia.434 F CH₂—OCH₃CH₂—CH═CH₂ Ia.435 Cl CH₂—OCH₃ CH₂—CH═CH₂ Ia.436 H CH₂—OCH₃ CH₂—C≡CHIa.437 F CH₂—OCH₃ CH₂—C≡CH Ia.438 Cl CH₂—OCH₃ CH₂—C≡CH Ia.439 H CH₂—OCH₃CH₂—CO—OCH₃ Ia.440 F CH₂—OCH₃ CH₂—CO—OCH₃ Ia.441 Cl CH₂—OCH₃ CH₂—CO—OCH₃Ia.442 H CH₂—OCH₃ CH₂-phenyl Ia.443 F CH₂—OCH₃ CH₂-phenyl Ia.444 ClCH₂—OCH₃ CH₂-phenyl Ia.445 H CH₂—CH₂—OCH₃ CH₃ Ia.446 F CH₂—CH₂—OCH₃ CH₃Ia.447 Cl CH₂—CH₂—OCH₃ CH₃ Ia.448 H CH₂—CH₂—OCH₃ C₂H₅ Ia.449 FCH₂—CH₂—OCH₃ C₂H₅ Ia.450 Cl CH₂—CH₂—OCH₃ C₂H₅ Ia.451 H CH₂—CH₂—OCH₃n-C₃H₇ Ia.452 F CH₂—CH₂—OCH₃ n-C₃H₇ Ia.453 Cl CH₂—CH₂—OCH₃ n-C₃H₇ Ia.454H CH₂—CH₂—OCH₃ n-C₄H₉ Ia.455 F CH₂—CH₂—OCH₃ n-C₄H₉ Ia.456 ClCH₂—CH₂—OCH₃ n-C₄H₉ Ia.457 H CH₂—CH₂—OCH₃ CH₂—CH═CH₂ Ia.458 FCH₂—CH₂—OCH₃ CH₂—CH═CH₂ Ia.459 Cl CH₂—CH₂—OCH₃ CH₂—CH═CH₂ Ia.460 HCH₂—CH₂—OCH₃ CH₂—C≡CH Ia.461 F CH₂—CH₂—OCH₃ CH₂—C≡CH Ia.462 ClCH₂—CH₂—OCH₃ CH₂—C≡CH Ia.463 H CH₂—CH₂—OCH₃ CH₂—CO—OCH₃ Ia.464 FCH₂—CH₂—OCH₃ CH₂—CO—OCH₃ Ia.465 Cl CH₂—CH₂—OCH₃ CH₂—CO—OCH₃ Ia.466 HCH₂—CH₂—OCH₃ CH₂-phenyl Ia.467 F CH₂—CH₂—OCH₃ CH₂-phenyl Ia.468 ClCH₂—CH₂—OCH₃ CH₂-phenyl la.469 H CH₂—CH₂—OCH₂—CH═CH₂ CH₃ Ia.470 FCH₂—CH₂—OCH₂—CH═CH₂ CH₃ Ia.471 Cl CH₂—CH₂—OCH₂—CH═CH₂ CH₃ Ia.472 HCH₂—CH₂—OCH₂—CH═CH₂ C₂H₅ Ia.473 F CH₂—CH₂—OCH₂—CH═CH₂ C₂H₅ Ia.474 ClCH₂—CH₂—OCH₂—CH═CH₂ C₂H₅ Ia.475 H CH₂—CH₂—OCH₂—CH═CH₂ n-C₃H₇ Ia.476 FCH₂—CH₂—OCH₂—CH═CH₂ n-C₃H₇ Ia.477 Cl CH₂—CH₂—OCH₂—CH═CH₂ n-C₃H₇ Ia.478 HCH₂—CH₂—OCH₂—CH═CH₂ n-C₄H₉ Ia.479 F CH₂—CH₂—OCH₂—CH═CH₂ n-C₄H₉ Ia.480 ClCH₂—CH₂—OCH₂—CH═CH₂ n-C₄H₉ Ia.481 H CH₂—CH₂—OCH₂—CH═CH₂ CH₂—CH═CH₂la.482 F CH₂—CH₂—OCH₂—CH═CH₂ CH₂—CH═CH₂ Ia.483 Cl CH₂—CH₂—OCH₂—CH═CH₂CH₂—CH═CH₂ Ia.484 H CH₂—CH₂—OCH₂—CH═CH₂ CH₂—C≡CH Ia.485 FCH₂—CH₂—OCH₂—CH═CH₂ CH₂—C≡CH Ia.486 Cl CH₂—CH₂—OCH₂—CH═CH₂ CH₂—C≡CHIa.487 H CH₂—CH₂—OCH₂—CH═CH₂ CH₂—CO—OCH₃ Ia.488 F CH₂—CH₂—OCH₂—CH═CH₂CH₂—CO—OCH₃ Ia.489 Cl CH₂—CH₂—OCH₂—CH═CH₂ CH₂—CO—OCH₃ Ia.490 HCH₂—CH₂—OCH₂—CH═CH₂ CH₂-phenyl Ia.491 F CH₂—CH₂—OCH₂—CH═CH₂ CH₂-phenylla.492 Cl CH₂—CH₂—OCH₂—CH═CH₂ CH₂-phenyl Ia.493 H CH₂—CH₂—O-cyclopentylCH₃ Ia.494 F CH₂—CH₂—O-cyclopentyl CH₃ Ia.495 Cl CH₂—CH₂—O-cyclopentylCH₃ Ia.496 H CH₂—CH₂—O-cyclopentyl C₂H₅ Ia.497 F CH₂—CH₂—O-cyclopentylC₂H₅ Ia.498 Cl CH₂—CH₂—O-cyclopentyl C₂H₅ Ia.499 H CH₂—CH₂—O-cyclopentyln-C₃H₇ Ia.500 F CH₂—CH₂—O-cyclopentyl n-C₃H₇ Ia.501 ClCH₂—CH₂—O-cyclopentyl n-C₃H₇ Ia.502 H CH₂—CH₂—O-cyclopentyl n-C₄H₉Ia.503 F CH₂—CH₂—O-cyclopentyl n-C₄H₉ Ia.504 Cl CH₂—CH₂—O-cyclopentyln-C₄H₉ Ia.505 H CH₂—CH₂—O-cyclopentyl CH₂—CH═CH₂ Ia.506 FCH₂—CH₂—O-cyclopentyl CH₂—CH═CH₂ Ia.507 Cl CH₂—CH₂—O-cyclopentylCH₂—CH═CH₂ Ia.508 H CH₂—CH₂—O-cyclopentyl CH₂—C≡CH Ia.509 FCH₂—CH₂—O-cyclopentyl CH₂—C≡CH Ia.510 Cl CH₂—CH₂—O-cyclopentyl CH₂—C≡CHIa.511 H CH₂—CH₂—O-cyclopentyl CH₂—CO—OCH₃ Ia.512 FCH₂—CH₂—O-cyclopentyl CH₂—CO—OCH₃ Ia.513 Cl CH₂—CH₂—O-cyclopentylCH₂—CO—OCH₃ Ia.514 H CH₂—CH₂—O-cyclopentyl CH₂-phenyl Ia.515 FCH₂—CH₂—O-cyclopentyl CH₂-phenyl la.516 Cl CH₂—CH₂—O-cyclopentylCH₂-phenyl Ia.517 H CH₂—CH₂—N(CH₃)₂ CH₃ Ia.518 F CH₂—CH₂—N(CH₃)₂ CH₃Ia.519 Cl CH₂—CH₂—N(CH₃)₂ CH₃ Ia.520 H CH₂—CH₂—N(CH₃)₂ C₂H₅ Ia.521 FCH₂—CH₂—N(CH₃)₂ C₂H₅ Ia.522 Cl CH₂—CH₂—N(CH₃)₂ C₂H₅ Ia.523 HCH₂—CH₂—N(CH₃)₂ n-C₃H₇ Ia.524 F CH₂—CH₂—N(CH₃)₂ n-C₃H₇ Ia.525 ClCH₂—CH₂—N(CH₃)₂ n-C₃H₇ Ia.526 H CH₂—CH₂—N(CH₃)₂ n-C₄H₉ Ia.527 FCH₂—CH₂—N(CH₃)₂ n-C₄H₉ Ia.528 Cl CH₂—CH₂—N(CH₃)₂ n-C₄H₉ Ia.529 HCH₂—CH₂—N(CH₃)₂ CH₂—CH═CH₂ Ia.530 F CH₂—CH₂—N(CH₃)₂ CH₂—CH═CH₂ Ia.531 ClCH₂—CH₂—N(CH₃)₂ CH₂—CH═CH₂ Ia.532 H CH₂—CH₂—N(CH₃)₂ CH₂—C≡CH Ia.533 FCH₂—CH₂—N(CH₃)₂ CH₂—C≡CH Ia.534 Cl CH₂—CH₂—N(CH₃)₂ CH₂—C≡CH Ia.535 HCH₂—CH₂—N(CH₃)₂ CH₂—CO—OCH₃ Ia.536 F CH₂—CH₂—N(CH₃)₂ CH₂—CO—OCH₃ Ia.537Cl CH₂—CH₂—N(CH₃)₂ CH₂—CO—OCH₃ Ia.538 H CH₂—CH₂—N(CH₃)₂ CH₂-phenylIa.539 F CH₂—CH₂—N(CH₃)₂ CH₂-phenyl Ia.540 Cl CH₂—CH₂—N(CH₃)₂ CH₂-phenylIa.541 H CH₂—CH₂—CH₃ CH₃ Ia.542 F CH₂—CH₂—CH₃ CH₃ Ia.543 Cl CH₂—CH₂—CH₃CH₃ Ia.544 H CH₂—CH₂—SCH₃ C₂H₅ Ia.545 F CH₂—CH₂—SCH₃ C₂H₅ Ia.546 ClCH₂—CH₂—SCH₃ C₂H₅ Ia.547 H CH₂—CH₂—SCH₃ n-C₃H₇ Ia.548 F CH₂—CH₂—SCH₃n-C₃H₇ Ia.549 Cl CH₂—CH₂—SCH₃ n-C₃H₇ Ia.550 H CH₂—CH₂—SCH₃ n-C₄H₉ Ia.551F CH₂—CH₂—SCH₃ n-C₄H₉ Ia.552 Cl CH₂—CH₂—SCH₃ n-C₄H₉ Ia.553 HCH₂—CH₂—SCH₃ CH₂—CH═CH₂ Ia.554 F CH₂—CH₂—SCH₃ CH₂—CH═CH₂ Ia.555 ClCH₂—CH₂—SCH₃ CH₂—CH═CH₂ Ia.556 H CH₂—CH₂—SCH₃ CH₂—C≡CH Ia.557 FCH₂—CH₂—SCH₃ CH₂—C≡CH Ia.558 Cl CH₂—CH₂—SCH₃ CH₂—C≡CH Ia.559 HCH₂—CH₂—SCH₃ CH₂—CO—OCH₃ Ia.560 F CH₂—CH₂—SCH₃ CH₂—CO—OCH₃ Ia.561 ClCH₂—CH₂—SCH₃ CH₂—CO—OCH₃ Ia.562 H CH₂—CH₂—SCH₃ CH₂-phenyl Ia.563 FCH₂—CH₂—SCH₃ CH₂-phenyl Ia.564 Cl CH₂—CH₂—SCH₃ CH₂-phenyl Ia.565 HCH₂—CH₂—SO₂—CH₃ CH₃ Ia.566 F CH₂—CH₂—SO₂—CH₃ CH₃ Ia.567 ClCH₂—CH₂—SO₂—CH₃ CH₃ Ia.568 H CH₂—CH₂—SO₂—CH₃ C₂H₅ Ia.569 FCH₂—CH₂—SO₂—CH₃ C₂H₅ Ia.570 Cl CH₂—CH₂—SO₂—CH₃ C₂H₅ Ia.571 HCH₂—CH₂—SO₂—CH₃ n-C₃H₇ Ia.572 F CH₂—CH₂—SO₂—CH₃ n-C₃H₇ Ia.573 ClCH₂—CH₂—SO₂—CH₃ n-C₃H₇ Ia.574 H CH₂—CH₂—SO₂—CH₃ n-C₄H₉ Ia.575 FCH₂—CH₂—SO₂—CH₃ n-C₄H₉ Ia.576 Cl CH₂—CH₂—SO₂—CH₃ n-C₄H₉ Ia.577 HCH₂—CH₂—SO₂—CH₃ CH₂—CH═CH₂ Ia.578 F CH₂—CH₂—SO₂—CH₃ CH₂—CH═CH₂ Ia.579 ClCH₂—CH₂—SO₂—CH₃ CH₂—CH═CH₂ Ia.580 H CH₂—CH₂—SO₂—CH₃ CH₂—C≡CH Ia.581 FCH₂—CH₂—SO₂—CH₃ CH₂—C≡CH Ia.582 Cl CH₂—CH₂—SO₂—CH₃ CH₂—C≡CH la.583 HCH₂—CH₂—SO₂—CH₃ CH₂—CO—OCH₃ Ia.584 F CH₂—CH₂—SO₂—CH₃ CH₂—CO—OCH₃ Ia.585Cl CH₂—CH₂—SO₂—CH₃ CH₂—CO—OCH₃ Ia.586 H CH₂—CH₂—SO₂—CH₃ CH₂-phenylIa.587 F CH₂—CH₂—SO₂—CH₃ CH₂-phenyl Ia.588 Cl CH₂—CH₂—SO₂—CH₃ CH₂-phenylIa.589 H CH₂—CH═CH₂ CH₃ Ia.590 F CH₂—CH═CH₂ CH₃ Ia.591 Cl CH₂—CH═CH₂ CH₃Ia.592 H CH₂—CH═CH₂ C₂H₅ Ia.593 F CH₂—CH═CH₂ C₂H₅ Ia.594 Cl CH₂—CH═CH₂C₂H₅ Ia.595 H CH₂—CH═CH₂ n-C₃H₇ Ia.596 F CH₂—CH═CH₂ n-C₃H₇ Ia.597 ClCH₂—CH═CH₂ n-C₃H₇ Ia.598 H CH₂—CH═CH₂ n-C₄H₉ Ia.599 F CH₂—CH═CH₂ n-C₄H₉Ia.600 Cl CH₂—CH═CH₂ n-C₄H₉ Ia.601 H CH₂—CH═CH₂ CH₂—CH═CH₂ Ia.602 FCH₂—CH═CH₂ CH₂—CH═CH₂ Ia.603 Cl CH₂—CH═CH₂ CH₂—CH═CH₂ Ia.604 HCH₂—CH═CH₂ CH₂—C≡CH Ia.605 F CH₂—CH═CH₂ CH₂—C≡CH Ia.606 Cl CH₂—CH═CH₂CH₂—C≡CH Ia.607 H CH₂—CH═CH₂ CH₂—CO—OCH₃ Ia.608 F CH₂—CH═CH₂ CH₂—CO—OCH₃Ia.609 Cl CH₂—CH═CH₂ CH₂—CO—OCH₃ Ia.610 H CH₂—CH═CH₂ CH₂-phenyl Ia.611 FCH₂—CH═CH₂ CH₂-phenyl Ia.612 Cl CH₂—CH═CH₂ CH₂-phenyl Ia.613 HCH₂—CH═CH—CH₃ CH₃ Ia.614 F CH₂—CH═CH—CH₃ CH₃ Ia.615 Cl CH₂—CH═CH—CH₃ CH₃Ia.616 H CH₂—CH═CH—CH₃ C₂H₅ Ia.617 F CH₂—CH═CH—CH₃ C₂H₅ Ia.618 ClCH₂—CH═CH—CH₃ C₂H₅ Ia.619 H CH₂—CH═CH—CH₃ n-C₃H₇ Ia.620 F CH₂—CH═CH—CH₃n-C₃H₇ Ia.621 Cl CH₂—CH═CH—CH₃ n-C₃H₇ Ia.622 H CH₂—CH═CH—CH₃ n-C₄H₉Ia.623 F CH₂—CH═CH—CH₃ n-C₄H₉ Ia.624 Cl CH₂—CH═CH—CH₃ n-C₄H₉ Ia.625 HCH₂—CH═CH—CH₃ CH₂—CH═CH₂ Ia.626 F CH₂—CH═CH—CH₃ CH₂—CH═CH₂ Ia.627 ClCH₂—CH═CH—CH₃ CH₂—CH═CH₂ Ia.628 H CH₂—CH═CH—CH₃ CH₂—C≡CH Ia.629 FCH₂—CH═CH—CH₃ CH₂—C≡CH Ia.631 F CH₂—CH═CH—CH₃ CH₂—CO—OCH₃ Ia.632 FCH₂—CH═CH—CH₃ CH₂—CO—OCH₃ Ia.633 Cl CH₂—CH═CH—CH₃ CH₂—CO—OCH₃ Ia.634 HCH₂—CH═CH—CH₃ CH₂—phenyl Ia.635 F CH₂—CH═CH—CH₃ CH₂—phenyl Ia.636 ClCH₂—CH═CH—CH₃ CH₂—phenyl Ia.637 H CH₂—CH═CH—Cl CH₃ Ia.638 F CH₂—CH═CH—ClCH₃ Ia.639 Cl CH₂—CH═CH—Cl CH₃ Ia.640 H CH₂—CH═CH—Cl C₂H₅ Ia.641 FCH₂—CH═CH—Cl C₂H₅ Ia.642 Cl CH₂—CH═CH—Cl C₂H₅ Ia.643 H CH₂—CH═CH—Cln-C₃H₇ Ia.644 F CH₂—CH═CH—Cl n-C₃H₇ Ia.645 Cl CH₂—CH═CH—Cl n-C₃H₇ Ia.646H CH₂—CH═CH—Cl n-C₄H₉ Ia.647 F CH₂—CH═CH—Cl n-C₄H₉ Ia.648 ClCH₂—CH═CH—Cl n-C₄H₉ Ia.649 H CH₂—CH═CH—Cl CH₂—CH═CH₂ Ia.650 FCH₂—CH═CH—Cl CH₂—CH═CH₂ Ia.651 Cl CH₂—CH═CH—Cl CH₂—CH═CH₂ Ia.652 HCH₂—CH═CH—Cl CH₂—C≡CH Ia.653 F CH₂—CH═CH—Cl CH₂—C≡CH Ia.654 ClCH₂—CH═CH—Cl CH₂—C≡CH Ia.655 H CH₂—CH═CH—Cl CH₂—CO—OCH₃ Ia.656 FCH₂—CH═CH—Cl CH₂—CO—OCH₃ Ia.657 Cl CH₂—CH═CH—Cl CH₂—CO—OCH₃ Ia.658 HCH₂—CH═CH—Cl CH₂-phenyl Ia.659 F CH₂—CH═CH—Cl CH₂-phenyl Ia.660 ClCH₂—CH═CH—Cl CH₂-phenyl Ia.661 H CH₂—C≡CH CH₃ Ia.662 F CH₂—C≡CH CH₃Ia.663 Cl CH₂—C≡CH CH₃ Ia.664 H CH₂—C≡CH C₂H₅ Ia.665 F CH₂—C≡CH C₂H₅Ia.666 Cl CH₂—C≡CH C₂H₅ Ia.667 H CH₂—C≡CH n-C₃H₇ Ia.668 F CH₂—C≡CHn-C₃H₇ Ia.669 Cl CH₂—C≡CH n-C₃H₇ Ia.670 H CH₂—C≡CH n-C₄H₉ Ia.671 FCH₂—C≡CH n-C₄H₉ Ia.672 Cl CH₂—C≡CH n-C₄H₉ Ia.673 H CH₂—C≡CH CH₂—CH═CH₂Ia.674 F CH₂—C≡CH CH₂—CH═CH₂ Ia.675 Cl CH₂—C≡CH CH₂—CH═CH₂ Ia.676 HCH₂—C≡CH CH₂—C≡CH Ia.677 F CH₂—C≡CH CH₂—C≡CH Ia.678 Cl CH₂—C≡CH CH₂—C≡CHIa.679 H CH₂—C≡CH CH₂—CO—OCH₃ Ia.680 F CH₂—C≡CH CH₂—CO—OCH₃ Ia.681 ClCH₂—C≡CH CH₂—CO—OCH₃ Ia.682 H CH₂—C≡CH CH₂-phenyl Ia.683 F CH₂—C≡CHCH₂-phenyl Ia.684 Cl CH₂—C≡CH CH₂-phenyl Ia.685 H CO—CH₃ CH₃ Ia.686 FCO—CH₃ CH₃ Ia.687 Cl CO—CH₃ CH₃ Ia.688 H CO—CH₃ C₂H₅ Ia.689 F CO—CH₃C₂H₅ Ia.690 Cl CO—CH₃ C₂H₅ Ia.691 H CO—CH₃ n-C₃H₇ Ia.692 F CO—CH₃ n-C₃H₇Ia.693 Cl CO—CH₃ n-C₃H₇ Ia.694 H CO—CH₃ n-C₄H₉ Ia.695 F CO—CH₃ n-C₄H₉Ia.696 Cl CO—CH₃ n-C₄H₉ Ia.697 H CO—CH₃ CH₂—CH═CH₂ Ia.698 F CO—CH₃CH₂—CH═CH₂ Ia.699 Cl CO—CH₃ CH₂—CH═CH₂ Ia.700 H CO—CH₃ CH₂—C≡CH Ia.701 FCO—CH₃ CH₂—C≡CH Ia.702 Cl CO—CH₃ CH₂—C≡CH Ia.703 H CO—CH₃ CH₂—CO—OCH₃Ia.704 F CO—CH₃ CH₂—CO—OCH₃ Ia.705 Cl CO—CH₃ CH₂—CO—OCH₃ Ia.706 H CO—CH₃CH₂-phenyl Ia.707 F CO—CH₃ CH₂-phenyl Ia.708 Cl CO—CH₃ CH₂-phenyl Ia.709H CO—C₂H₅ CH₃ Ia.710 F CO—C₂H₅ CH₃ Ia.711 Cl CO—C₂H₅ CH₃ Ia.712 HCO—C₂H₅ C₂H₅ Ia.713 F CO—C₂H₅ C₂H₅ Ia.714 Cl CO—C₂H₅ C₂H₅ Ia.715 HCO—C₂H₅ n-C₃H₇ Ia.716 F CO—C₂H₅ n-C₃H₇ Ia.717 Cl CO—C₂H₅ n-C₃H₇ Ia.718 HCO—C₂H₅ n-C₄H₉ Ia.719 F CO—C₂H₅ n-C₄H₉ Ia.720 Cl CO—C₂H₅ n-C₄H₉ Ia.721 HCO—C₂H₅ CH₂—CH═CH₂ Ia.722 F CO—C₂H₅ CH₂—CH═CH₂ Ia.723 Cl CO—C₂H₅CH₂—CH═CH₂ Ia.724 H CO—C₂H₅ CH₂—C≡CH Ia.725 F CO—C₂H₅ CH₂—C≡CH Ia.726 ClCO—C₂H₅ CH₂—C≡CH Ia.727 H CO—C₂H₅ CH₂—CO—OCH₃ Ia.728 F CO—C₂H₅CH₂—CO—OCH₃ Ia.729 Cl CO—C₂H₅ CH₂—CO—OCH₃ Ia.730 H CO—C₂H₅ CH₂-phenylIa.731 F CO—C₂H₅ CH₂-phenyl Ia.732 Cl CO—C₂H₅ CH₂-phenyl Ia.733 HCO—CH₂Cl CH₃ Ia.734 F CO—CH₂Cl CH₃ Ia.735 Cl CO—CH₂Cl CH₃ Ia.736 HCO—CH₂Cl C₂H₅ Ia.737 F CO—CH₂Cl C₂H₅ Ia.738 Cl CO—CH₂Cl C₂H₅ la.739 HCO—CH₂Cl n-C₃H₇ Ia.740 F CO—CH₂Cl n-C₃H₇ Ia.741 Cl CO—CH₂Cl n-C₃H₇la.742 H CO—CH₂Cl n-C₄H₉ Ia.743 F CO—CH₂Cl n-C₄H₉ Ia.744 Cl CO—CH₂Cln-C₄H₉ Ia.745 H CO—CH₂Cl CH₂—CH═CH₂ Ia.746 F CO—CH₂Cl CH₂—CH═CH₂ Ia.747Cl CO—CH₂Cl CH₂—CH═CH₂ Ia.748 H CO—CH₂Cl CH₂—C≡CH Ia.749 F CO—CH₂ClCH₂—C≡CH Ia.750 Cl CO—CH₂Cl CH₂—C≡CH Ia.751 H CO—CH₂Cl CH₂—CO—OCH₃Ia.752 F CO—CH₂Cl CH₂—CO—OCH₃ Ia.753 Cl CO—CH₂Cl CH₂—CO—OCH₃ Ia.754 HCO—CH₂Cl CH₂-phenyl Ia.755 F CO—CH₂Cl CH₂-phenyl Ia.756 Cl CO—CH₂ClCH₂-phenyl Ia.757 H CO—CF₃ CH₃ Ia.758 F CO—CF₃ CH₃ Ia.759 Cl CO—CF₃ CH₃Ia.760 H CO—CF₃ C₂H₅ Ia.761 F CO—CF₃ C₂H₅ Ia.762 Cl CO—CF₃ C₂H₅ Ia.763 HCO—CF₃ n-C₃H₇ Ia.764 F CO—CF₃ n-C₃H₇ Ia.765 Cl CO—CF₃ n-C₃H₇ Ia.766 HCO—CF₃ n-C₄H₉ Ia.767 F CO—CF₃ n-C₄H₉ Ia.768 Cl CO—CF₃ n-C₄H₉ Ia.769 HCO—CF₃ CH₂—CH═CH₂ Ia.770 F CO—CF₃ CH₂—CH═CH₂ Ia.771 Cl CO—CF₃ CH₂—CH═CH₂Ia.772 H CO—CF₃ CH₂—C≡CH Ia.773 F CO—CF₃ CH₂—C≡CH Ia.774 Cl CO—CF₃CH₂—C≡CH Ia.775 H CO—CF₃ CH₂—CO—OCH₃ Ia.776 F CO—CF₃ CH₂—CO—OCH₃ Ia.777Cl CO—CF₃ CH₂—CO—OCH₃ Ia.778 H CO—CF₃ CH₂-phenyl Ia.779 F CO—CF₃CH₂-phenyl Ia.780 Cl CO—CF₃ CH₂-phenyl Ia.781 H CO—OCH₃ CH₃ Ia.782 FCO—OCH₃ CH₃ Ia.783 Cl CO—OCH₃ CH₃ Ia.784 H CO—OCH₃ C₂H₅ Ia.785 F CO—OCH₃C₂H₅ Ia.786 Cl CO—OCH₃ C₂H₅ la.787 H CO—OCH₃ n-C₃H₇ Ia.788 F CO—OCH₃n-C₃H₇ Ia.789 Cl CO—OCH₃ n-C₃H₇ Ia.790 H CO—OCH₃ n-C₄H₉ Ia.791 F CO—OCH₃n-C₄H₉ Ia.792 Cl CO—OCH₃ n-C₄H₉ Ia.793 H CO—OCH₃ CH₂—CH═CH₂ Ia.794 FCO—OCH₃ CH₂—CH═CH₂ Ia.795 Cl CO—OCH₃ CH₂—CH═CH₂ Ia.796 H CO—OCH₃CH₂—C≡CH Ia.797 F CO—OCH₃ CH₂—C≡CH Ia.798 Cl CO—OCH₃ CH₂—C≡CH Ia.799 HCO—OCH₃ CH₂—CO—OCH₃ Ia.800 F CO—OCH₃ CH₂—CO—OCH₃ Ia.801 Cl CO—OCH₃CH₂—CO—OCH₃ Ia.802 H CO—OCH₃ CH₂-phenyl Ia.803 F CO—OCH₃ CH₂-phenylIa.804 Cl CO—OCH₃ CH₂-phenyl Ia.805 H CO—OC₂H₅ CH₃ Ia.806 F CO—OC₂H₅ CH₃Ia.807 Cl CO—OC₂H₅ CH₃ Ia.808 H CO—OC₂H₅ C₂H₅ Ia.809 F CO—OC₂H₅ C₂H₅Ia.810 Cl CO—OC₂H₅ C₂H₅ Ia.811 H CO—OC₂H₅ n-C₃H₇ Ia.812 F CO—OC₂H₅n-C₃H₇ Ia.813 Cl CO—OC₂H₅ n-C₃H₇ Ia.814 H CO—OC₂H₅ n-C₄H₉ Ia.815 FCO—OC₂H₅ n-C₄H₉ Ia.816 Cl CO—OC₂H₅ n-C₄H₉ Ia.817 H CO—OC₂H₅ CH₂—CH═CH₂Ia.818 F CO—OC₂H₅ CH₂—CH═CH₂ Ia.819 Cl CO—OC₂H₅ CH₂—CH═CH₂ Ia.820 HCO—OC₂H₅ CH₂—C≡CH Ia.821 F CO—OC₂H₅ CH₂—C≡CH Ia.822 Cl CO—OC₂H₅ CH₂—C≡CHIa.823 H CO—OC₂H₅ CH₂—CO—OCH₃ Ia.824 F CO—OC₂H₅ CH₂—CO—OCH₃ Ia.825 ClCO—OC₂H₅ CH₂—CO—OCH₃ Ia.826 H CO—OC₂H₅ CH₂-phenyl Ia.827 F CO—OC₂H₅CH₂-phenyl Ia.828 Cl CO—OC₂H₅ CH₂-phenyl Ia.829 H CO—N(CH₃)₂ CH₃ Ia.830F CO—N(CH₃)₂ CH₃ Ia.831 Cl CO—N(CH₃)₂ CH₃ Ia.832 H CO—N(CH₃)₂ C₂H₅Ia.833 F CO—N(CH₃)₂ C₂H₅ Ia.834 Cl CO—N(CH₃)₂ C₂H₅ Ia.835 H CO—N(CH₃)₂n-C₃H₇ Ia.836 F CO—N(CH₃)₂ n-C₃H₇ Ia.837 Cl CO—N(CH₃)₂ n-C₃H₇ Ia.838 HCO—N(CH₃)₂ n-C₄H₉ Ia.839 F CO—N(CH₃)₂ n-C₄H₉ Ia.840 Cl CO—N(CH₃)₂ n-C₄H₉Ia.841 H CO—N(CH₃)₂ CH₂—CH═CH₂ Ia.842 F CO—N(CH₃)₂ CH₂—CH═CH₂ Ia.843 ClCO—N(CH₃)₂ CH₂—CH═CH₂ Ia.844 H CO—N(CH₃)₂ CH₂—C≡CH Ia.845 F CO—N(CH₃)₂CH₂—C≡CH Ia.846 Cl CO—N(CH₃)₂ CH₂—C≡CH Ia.847 H CO—N(CH₃)₂ CH₂—CO—OCH₃Ia.848 F CO—N(CH₃)₂ CH₂—CO—OCH₃ Ia.849 Cl CO—N(CH₃)₂ CH₂—CO—OCH₃ Ia.850H CO—N(CH₃)₂ CH₂-phenyl Ia.851 F CO—N(CH₃)₂ CH₂-phenyl Ia.852 ClCO—N(CH₃)₂ CH₂-phenyl Ia.853 H CO—N(C₂H₅)₂ CH₃ Ia.854 F CO—N(C₂H₅)₂ CH₃Ia.855 Cl CO—N(C₂H₅)₂ CH₃ Ia.856 H CO—N(C₂H₅)₂ C₂H₅ Ia.857 F CO—N(C₂H₅)₂C₂H₅ Ia.858 Cl CO—N(C₂H₅)₂ C₂H₅ Ia.859 H CO—N(C₂H₅)₂ n-C₃H₇ Ia.860 FCO—N(C₂H₅)₂ n-C₃H₇ Ia.861 Cl CO—N(C₂H₅)₂ n-C₃H₇ Ia.862 H CO—N(C₂H₅)₂n-C₄H₉ Ia.863 F CO—N(C₂H₅)₂ n-C₄H₉ Ia.864 Cl CO—N(C₂H₅)₂ n-C₄H₉ Ia.865 HCO—N(C₂H₅)₂ CH₂—CH═CH₂ Ia.866 F CO—N(C₂H₅)₂ CH₂—CH═CH₂ Ia.867 ClCO—N(C₂H₅)₂ CH₂—CH═CH₂ Ia.868 H CO—N(C₂H₅)₂ CH₂—C≡CH Ia.869 FCO—N(C₂H₅)₂ CH₂—C≡CH Ia.870 Cl CO—N(C₂H₅)₂ CH₂—C≡CH Ia.871 H CO—N(C₂H₅)₂CH₂—CO—OCH₃ Ia.872 F CO—N(C₂H₅)₂ CH₂—CO—OCH₃ Ia.873 Cl CO—N(C₂H₅)₂CH₂—CO—OCH₃ Ia.874 H CO—N(C₂H₅)₂ CH₂-phenyl Ia.875 F CO—N(C₂H₅)₂CH₂-phenyl Ia.876 Cl CO—N(C₂H₅)₂ CH₂-phenyl Ia.877 H SO₂—CH₃ CH₃ Ia.878F SO₂—CH₃ CH₃ Ia.879 Cl SO₂—CH₃ CH₃ Ia.880 H SO₂—CH₃ C₂H₅ Ia.881 FSO₂—CH₃ C₂H₅ Ia.882 Cl SO₂—CH₃ C₂H₅ Ia.883 H SO₂—CH₃ n-C₃H₇ Ia.884 FSO₂—CH₃ n-C₃H₇ Ia.885 Cl SO₂—CH₃ n-C₃H₇ Ia.886 H SO₂—CH₃ n-C₄H₉ Ia.887 FSO₂—CH₃ n-C₄H₉ Ia.888 Cl SO₂—CH₃ n-C₄H₉ Ia.889 H SO₂—CH₃ CH₂—CH═CH₂Ia.890 F SO₂—CH₃ CH₂—CH═CH₂ Ia.891 Cl SO₂—CH₃ CH₂—CH═CH₂ Ia.892 HSO₂—CH₃ CH₂—C≡CH Ia.893 F SO₂—CH₃ CH₂—C≡CH Ia.894 Cl SO₂—CH₃ CH₂—C≡CHIa.895 H SO₂—CH₃ CH₂—CO—OCH₃ Ia.896 F SO₂—CH₃ CH₂—CO—OCH₃ Ia.897 ClSO₂—CH₃ CH₂—CO—OCH₃ Ia.898 H SO₂—CH₃ CH₂-phenyl Ia.899 F SO₂—CH₃CH₂-phenyl Ia.900 Cl SO₂—CH₃ CH₂-phenyl Ia.901 H CH₂—CO—CH₃ CH₃ Ia.902 pCH₂—CO—CH₃ CH₃ Ia.903 Cl CH₂—CO—CH₃ CH₃ Ia.904 H CH₂—CO—CH₃ C₂H₅ Ia.905F CH₂—CO—CH₃ C₂H₅ Ia.906 Cl CH₂—CO—CH₃ C₂H₅ Ia.907 H CH₂—CO—CH₃ n-C₃H₇Ia.908 F CH₂—CO—CH₃ n-C₃H₇ Ia.909 Cl CH₂—CO—CH₃ n-C₃H₇ Ia.910 HCH₂—CO—CH₃ n-C₄H₉ Ia.911 F CH₂—CO—CH₃ n-C₄H₉ Ia.912 Cl CH₂—CO—CH₃ n-C₄H₉Ia.913 H CH₂—CO—CH₃ CH₂—CH═CH₂ Ia.914 F CH₂—CO—CH₃ CH₂—CH═CH₂ Ia.915 ClCH₂—CO—CH₃ CH₂—CH═CH₂ Ia.916 H CH₂—CO—CH₃ CH₂—C≡CH Ia.917 F CH₂—CO—CH₃CH₂—C≡CH Ia.918 Cl CH₂—CO—CH₃ CH₂—C≡CH Ia.919 H CH₂—CO—CH₃ CH₂—CO—OCH₃Ia.920 F CH₂—CO—CH₃ CH₂—CO—OCH₃ Ia.921 Cl CH₂—CO—CH₃ CH₂—CO—OCH₃ Ia.922H CH₂—CO—CH₃ CH₂-phenyl Ia.923 F CH₂—CO—CH₃ CH₂-phenyl Ia.924 ClCH₂—CO—CH₃ CH₂-phenyl Ia.925 H CH₂—CO—C₂H₅ CH₃ Ia.926 F CH₂—CO—C₂H₅ CH₃Ia.927 Cl CH₂—CO—C₂H₅ CH₃ Ia.928 H CH₂—CO—C₂H₅ C₂H₅ Ia.929 F CH₂—CO—C₂H₅C₂H₅ Ia.930 Cl CH₂—CO—C₂H₅ C₂H₅ Ia.931 H CH₂—CO—C₂H₅ n-C₃H₇ Ia.932 FCH₂—CO—C₂H₅ n-C₃H₇ Ia.933 Cl CH₂—CO—C₂H₅ n-C₃H₇ Ia.934 H CH₂—CO—C₂H₅n-C₄H₉ Ia.935 F CH₂—CO—C₂H₅ n-C₄H₉ Ia.936 Cl CH₂—CO—C₂H₅ n-C₄H₉ Ia.937 HCH₂—CO—C₂H₅ CH₂—CH═CH₂ Ia.938 F CH₂—CO—C₂H₅ CH₂—CH═CH₂ Ia.939 ClCH₂—CO—C₂H₅ CH₂—CH═CH₂ Ia.940 H CH₂—CO—C₂H₅ CH₂—C≡CH Ia.941 FCH₂—CO—C₂H₅ CH₂—C≡CH Ia.942 Cl CH₂—CO—C₂H₅ CH₂—C≡CH Ia.943 H CH₂—CO—C₂H₅CH₂—CO—OCH₃ Ia.944 F CH₂—CO—C₂H₅ CH₂—CO—OCH₃ Ia.945 Cl CH₂—CO—C₂H₅CH₂—CO—OCH₃ Ia.946 H CH₂—CO—C₂H₅ CH₂-phenyl Ia.947 F CH₂—CO—C₂H₅CH₂-phenyl Ia.948 Cl CH₂—CO—C₂H₅ CH₂-phenyl Ia.949 H CH₂—CO—CH₂Cl CH₃Ia.950 F CH₂—CO—CH₂Cl CH₃ Ia.951 Cl CH₂—CO—CH₂Cl CH₃ Ia.952 HCH₂—CO—CH₂Cl C₂H₅ Ia.953 F CH₂—CO—CH₂Cl C₂H₅ Ia.954 Cl CH₂—CO—CH₂Cl C₂H₅Ia.955 H CH₂—CO—CH₂Cl n-C₃H₇ Ia.956 F CH₂—CO—CH₂Cl n-C₃H₇ Ia.957 ClCH₂—CO—CH₂Cl n-C₃H₇ Ia.958 H CH₂—CO—CH₂Cl n-C₄H₉ Ia.959 F CH₂—CO—CH₂Cln-C₄H₉ Ia.960 Cl CH₂—CO—CH₂Cl n-C₄H₉ Ia.961 H CH₂—CO—CH₂Cl CH₂—CH═CH₂Ia.962 F CH₂—CO—CH₂Cl CH₂—CH═CH₂ Ia.963 Cl CH₂—CO—CH₂Cl CH₂—CH═CH₂la.964 H CH₂—CO—CH₂Cl CH₂—C≡CH Ia.965 F CH₂—CO—CH₂Cl CH₂—C≡CH Ia.966 ClCH₂—CO—CH₂Cl CH₂—C≡CH Ia.967 H CH₂—CO—CH₂Cl CH₂—CO—OCH₃ Ia.968 FCH₂—CO—CH₂Cl CH₂—CO—OCH₃ Ia.969 Cl CH₂—CO—CH₂Cl CH₂—CO—OCH₃ Ia.970 HCH₂—CO—CH₂Cl CH₂-phenyl Ia.971 F CH₂—CO—CH₂Cl CH₂-phenyl Ia.972 ClCH₂—CO—CH₂Cl CH₂-phenyl Ia.973 H CH₂—CO—CF₃ CH₃ Ia.974 F CH₂—CO—CF₃ CH₃Ia.975 Cl CH₂—CO—CF₃ CH₃ Ia.976 H CH₂—CO—CF₃ C₂H₅ Ia.977 F CH₂—CO—CF₃C₂H₅ Ia.978 Cl CH₂—CO—CF₃ C₂H₅ Ia.979 H CH₂—CO—CF₃ n-C₃H₇ Ia.980 FCH₂—CO—CF₃ n-C₃H₇ Ia.981 Cl CH₂—CO—CF₃ n-C₃H₇ Ia.982 H CH₂—CO—CF₃ n-C₄H₉Ia.983 F CH₂—CO—CF₃ n-C₄H₉ Ia.984 Cl CH₂—CO—CF₃ n-C₄H₉ Ia.985 HCH₂—CO—CF₃ CH₂—CH═CH₂ Ia.986 F CH₂—CO—CF₃ CH₂—CH═CH₂ Ia.987 ClCH₂—CO—CF₃ CH₂—CH═CH₂ Ia.988 H CH₂—CO—CF₃ CH₂—C≡CH Ia.989 F CH₂—CO—CF₃CH₂—C≡CH Ia.990 Cl CH₂—CO—CF₃ CH₂—C≡CH Ia.991 H CH₂—CO—CF₃ CH₂—CO—OCH₃Ia.992 F CH₂—CO—CF₃ CH₂—CO—OCH₃ Ia.993 Cl CH₂—CO—CF₃ CH₂—CO—OCH₃ Ia.994H CH₂—CO—CF₃ CH₂-phenyl Ia.995 F CH₂—CO—CF₃ CH₂-phenyl Ia.996 ClCH₂—CO—CF₃ CH₂-phenyl Ia.997 H CH₂—CO-cyclopropyl CH₃ Ia.998 FCH₂—CO-cyclopropyl CH₃ Ia.999 Cl CH₂—CO-cyclopropyl CH₃ Ia.1000 HCH₂—CO-cyclopropyl C₂H₅ Ia.1001 F CH₂—CO-cyclopropyl C₂H₅ Ia.1002 ClCH₂—CO-cyclopropyl C₂H₅ Ia.1003 H CH₂—CO-cyclopropyl n-C₃H₇ Ia.1004 FCH₂—CO-cyclopropyl n-C₃H₇ Ia.1005 Cl CH₂—CO-cyclopropyl n-C₃H₇ Ia.1006 HCH₂—CO-cyclopropyl n-C₄H₉ Ia.1007 F CH₂—CO-cyclopropyl n-C₄H₉ Ia.1008 ClCH₂—CO-cyclopropyl n-C₄H₉ Ia.1009 H CH₂—CO-cyclopropyl CH₂—CH═CH₂Ia.1010 F CH₂—CO-cyclopropyl CH₂—CH═CH₂ Ia.1011 Cl CH₂—CO-cyclopropylCH₂—CH═CH₂ Ia.1012 H CH₂—CO-cyclopropyl CH₂—C≡CH Ia.1013 FCH₂—CO-cyclopropyl CH₂—C≡CH Ia.1014 Cl CH₂—CO-cyclopropyl CH₂—C≡CHIa.1015 H CH₂—CO-cyclopropyl CH₂—CO—OCH₃ Ia.1016 F CH₂—CO-cyclopropylCH₂—CO—OCH₃ Ia.1017 Cl CH₂—CO-cyclopropyl CH₂—CO—OCH₃ Ia.1018 HCH₂—CO-cyclopropyl CH₂-phenyl Ia.1019 F CH₂—CO-cyclopropyl CH₂-phenylIa.1020 Cl CH₂—CO-cyclopropyl CH₂-phenyl Ia.1021 H CH₂—CO-cyclobutyl CH₃Ia.1022 F CH₂—CO-cyclobutyl CH₃ Ia.1023 Cl CH₂—CO-cyclobutyl CH₃ Ia.1024H CH₂—CO-cyclobutyl C₂H₅ Ia.1025 F CH₂—CO-cyclobutyl C₂H₅ la.1026 ClCH₂—CO-cyclobutyl C₂H₅ Ia.1027 H CH₂—CO-cyclobutyl n-C₃H₇ Ia.1028 FCH₂—CO-cyclobutyl n-C₃H₇ Ia.1029 Cl CH₂—CO-cyclobutyl n-C₃H₇ Ia.1030 HCH₂—CO-cyclobutyl n-C₄H₉ Ia.1031 F CH₂—CO-cyclobutyl n-C₄H₉ Ia.1032 ClCH₂—CO-cyclobutyl n-C₄H₉ Ia.1033 H CH₂—CO-cyclobutyl CH₂—CH═CH₂ Ia.1034F CH₂—CO-cyclobutyl CH₂—CH═CH₂ Ia.1035 Cl CH₂—CO-cyclobutyl CH₂—CH═CH₂Ia.1036 H CH₂—CO-cyclobutyl CH₂—C≡CH Ia.1037 F CH₂—CO-cyclobutylCH₂—C≡CH Ia.1038 Cl CH₂—CO-cyclobutyl CH₂—C≡CH Ia.1039 HCH₂—CO-cyclobutyl CH₂—CO—OCH₃ Ia.1040 F CH₂—CO-cyclobutyl CH₂—CO—OCH₃Ia.1041 Cl CH₂—CO-cyclobutyl CH₂—CO—OCH₃ Ia.1042 H CH₂—CO-cyclobutylCH₂-phenyl Ia.1043 F CH₂—CO-cyclobutyl CH₂-phenyl Ia.1044 ClCH₂—CO-cyclobutyl CH₂-phenyl Ia.1045 H CH₂—CO-cyclopentyl CH₃ Ia.1046 FCH₂—CO-cyclopentyl CH₃ Ia.1047 Cl CH₂—CO-cyclopentyl CH₃ Ia.1048 HCH₂—CO-cyclopentyl C₂H₅ Ia.1049 F CH₂—CO-cyclopentyl C₂H₅ Ia.2099 ClCH₂—CO-cyclopentyl C₂H₅ Ia.2100 H CH₂—CO-cyclopentyl n-C₃H₇ Ia.2101 FCH₂—CO-cyclopentyl n-C₃H₇ Ia.2102 Cl CH₂—CO-cyclopentyl n-C₃H₇ Ia.2103 HCH₂—CO-cyclopentyl n-C₄H₉ Ia.2104 F CH₂—CO-cyclopentyl n-C₄H₉ Ia.2105 ClCH₂—CO-cyclopentyl n-C₄H₉ Ia.2106 H CH₂—CO-cyclopentyl CH₂—CH═CH₂Ia.2107 F CH₂—CO-cyclopentyl CH₂—CH═CH₂ Ia.2108 Cl CH₂—CO-cyclopentylCH₂—CH═CH₂ Ia.2109 H CH₂—CO-cyclopentyl CH₂—C≡CH Ia.2110 FCH₂—CO-cyclopentyl CH₂—C≡CH Ia.2111 Cl CH₂—CO-cyclopentyl CH₂—C≡CHIa.2112 H CH₂—CO-cyclopentyl CH₂—CO—OCH₃ Ia.2113 F CH₂—CO-cyclopentylCH₂—CO—OCH₃ Ia.2114 Cl CH₂—CO-cyclopentyl CH₂—CO—OCH₃ Ia.2115 HCH₂—CO-cyclopentyl CH₂-phenyl Ia.2116 F CH₂—CO-cyclopentyl CH₂-phenylIa.2117 Cl CH₂—CO-cyclopentyl CH₂-phenyl Ia.2118 H CH₂—CO-cyclohexyl CH₃Ia.2119 F CH₂—CO-cyclohexyl CH₃ Ia.2120 Cl CH₂—CO-cyclohexyl CH₃ Ia.2121H CH₂—CO-cyclohexyl C₂H₅ Ia.2122 F CH₂—CO-cyclohexyl C₂H₅ Ia.2123 ClCH₂—CO-cyclohexyl C₂H₅ la.2124 H CH₂—CO-cyclohexyl n-C₃H₇ Ia.2125 FCH₂—CO-cyclohexyl n-C₃H₇ Ia.2126 Cl CH₂—CO-cyclohexyl n-C₃H₇ Ia.2127 HCH₂—CO-cyclohexyl n-C₄H₉ Ia.2128 F CH₂—CO-cyclohexyl n-C₄H₉ Ia.2129 ClCH₂—CO-cyclohexyl n-C₄H₉ Ia.2130 H CH₂—CO-cyclohexyl CH₂—CH═CH₂ Ia.2131F CH₂—CO-cyclohexyl CH₂—CH═CH₂ Ia.2132 Cl CH₂—CO-cyclohexyl CH₂—CH═CH₂Ia.2133 H CH₂—CO-cyclohexyl CH₂—C≡CH Ia.2134 F CH₂—CO-cyclohexylCH₂—C≡CH Ia.2135 Cl CH₂—CO-cyclohexyl CH₂—C≡CH Ia.2136 HCH₂—CO-cyclohexyl CH₂—CO—OCH₃ Ia.2137 F CH₂—CO-cyclohexyl CH₂—CO—OCH₃Ia.2138 Cl CH₂—CO-cyclohexyl CH₂—CO—OCH₃ Ia.2139 H CH₂—CO-cyclohexylCH₂-phenyl Ia.2140 F CH₂—CO-cyclohexyl CH₂-phenyl Ia.2141 ClCH₂—CO-cyclohexyl CH₂-phenyl Ia.2142 H CH₂—CH═N—OCH₃ CH₃ Ia.2143 FCH₂—CH═N—OCH₃ CH₃ Ia.2144 Cl CH₂—CH═N—OCH₃ CH₃ Ia.2145 H CH₂—CH═N—OCH₃C₂H₅ Ia.2146 F CH₂—CH═N—OCH₃ C₂H₅ Ia.2147 Cl CH₂—CH═N—OCH₃ C₂H₅ Ia.2148H CH₂—CH═N—OCH₃ n-C₃H₇ Ia.2149 F CH₂—CH═N—OCH₃ n-C₃H₇ Ia.2150 ClCH₂—CH═N—OCH₃ n-C₃H₇ Ia.2151 H CH₂—CH═N—OCH₃ n-C₄H₉ Ia.2152 FCH₂—CH═N—OCH₃ n-C₄H₉ Ia.2153 Cl CH₂—CH═N—OCH₃ n-C₄H₉ Ia.2154 HCH₂—CH═N—OCH₃ CH₂—CH═CH₂ Ia.2155 F CH₂—CH═N—OCH₃ CH₂—CH═CH₂ Ia.2156 ClCH₂—CH═N—OCH₃ CH₂—CH═CH₂ Ia.2157 H CH₂—CH═N—OCH₃ CH₂—C≡CH Ia.2158 FCH₂—CH═N—OCH₃ CH₂—C≡CH Ia.2159 Cl CH₂—CH═N—OCH₃ CH₂—C≡CH Ia.2160 HCH₂—CH═N—OCH₃ CH₂—CO—OCH₃ Ia.2161 F CH₂—CH═N—OCH₃ CH₂—CO—OCH₃ Ia.2162 ClCH₂—CH═N—OCH₃ CH₂—CO—OCH₃ Ia.2163 H CH₂—CH═N—OCH₃ CH₂-phenyl Ia.2164 FCH₂—CH═N—OCH₃ CH₂-phenyl Ia.2165 Cl CH₂—CH═N—OCH₃ CH₂-phenyl Ia.2166 HCH₂—CH═N—OC₂H₅ CH₃ Ia.2167 F CH₂—CH═N—OC₂H₅ CH₃ Ia.2168 ClCH₂—CH═N—OC₂H₅ CH₃ Ia.2169 H CH₂—CH═N—OC₂H₅ C₂H₅ Ia.2170 FCH₂—CH═N—OC₂H₅ C₂H₅ Ia.2171 Cl CH₂—CH═N—OC₂H₅ C₂H₅ Ia.2172 HCH₂—CH═N—OC₂H₅ n-C₃H₇ Ia.2173 F CH₂—CH═N—OC₂H₅ n-C₃H₇ Ia.2174 ClCH₂—CH═N—OC₂H₅ n-C₃H₇ Ia.2175 H CH₂—CH═N—OC₂H₅ n-C₄H₉ Ia.2176 FCH₂—CH═N—OC₂H₅ n-C₄H₉ Ia.2177 Cl CH₂—CH═N—OC₂H₅ n-C₄H₉ Ia.2178 HCH₂—CH═N—OC₂H₅ CH₂—CH═CH₂ Ia.2179 F CH₂—CH═N—OC₂H₅ CH₂—CH═CH₂ Ia.2180 ClCH₂—CH═N—OC₂H₅ CH₂—CH═CH₂ Ia.2181 H CH₂—CH═N—OC₂H₅ CH₂—C≡CH Ia.2182 FCH₂—CH═N—OC₂H₅ CH₂—C≡CH Ia.2183 Cl CH₂—CH═N—OC₂H₅ CH₂—C≡CH Ia.2184 HCH₂—CH═N—OC₂H₅ CH₂—CO—OCH₃ Ia.2185 F CH₂—CH═N—OC₂H₅ CH₂—CO—OCH₃ Ia.2186Cl CH₂—CH═N—OC₂H₅ CH₂—CO—OCH₃ Ia.2187 H CH₂—CH═N—OC₂H₅ CH₂-phenylIa.2188 F CH₂—CH═N—OC₂H₅ CH₂-phenyl Ia.2189 Cl CH₂—CH═N—OC₂H₅ CH₂-phenylIa.2190 H CH₂—CH═N—O(n-C₃H₇) CH₃ Ia.2191 F CH₂—CH═N—O(n-C₃H₇) CH₃Ia.2192 Cl CH₂—CH═N—O(n-C₃H₇) CH₃ Ia.2193 H CH₂—CH═N—O(n-C₃H₇) C₂H₅Ia.2194 F CH₂—CH═N—O(n-C₃H₇) C₂H₅ Ia.2195 Cl CH₂—CH═N—O(n-C₃H₇) C₂H₅Ia.2196 H CH₂—CH═N—O(n-C₃H₇) n-C₃H₇ Ia.2197 F CH₂—CH═N—O(n-C₃H₇) n-C₃H₇Ia.2198 Cl CH₂—CH═N—O(n-C₃H₇) n-C₃H₇ Ia.2199 H CH₂—CH═N—O(n-C₃H₇) n-C₄H₉Ia.2200 F CH₂—CH═N—O(n-C₃H₇) n-C₄H₉ Ia.2201 Cl CH₂—CH═N—O(n-C₃H₇) n-C₄H₉Ia.2202 H CH₂—CH═N—O(n-C₃H₇) CH₂—CH═CH₂ Ia.2203 F CH₂—CH═N—O(n-C₃H₇)CH₂—CH═CH₂ Ia.2204 Cl CH₂—CH═N—O(n-C₃H₇) CH₂—CH═CH₂ Ia.2205 HCH₂—CH═N—O(n-C₃H₇) CH₂—C≡CH Ia.2206 F CH₂—CH═N—O(n-C₃H₇) CH₂—C≡CHIa.2207 Cl CH₂—CH═N—O(n-C₃H₇) CH₂—C≡CH Ia.2208 H CH₂—CH═N—O(n-C₃H₇)CH₂—CO—OCH₃ Ia.2209 F CH₂—CH═N—O(n-C₃H₇) CH₂—CO—OCH₃ Ia.2210 ClCH₂—CH═N—O(n-C₃H₇) CH₂—CO—OCH₃ Ia.2211 H CH₂—CH═N—O(n-C₃H₇) CH₂-phenylIa.2212 F CH₂—CH═N—O(n-C₃H₇) CH₂-phenyl Ia.2213 Cl CH₂—CH═N—O(n-C₃H₇)CH₂-phenyl Ia.2214 H CH₂—CH═N—O(n-C₄H₉) CH₃ Ia.2215 F CH₂—CH═N—O(n-C₄H₉)CH₃ Ia.2216 Cl CH₂—CH═N—O(n-C₄H₉) CH₃ Ia.2217 H CH₂—CH═N—O(n-C₄H₉) C₂H₅Ia.2218 F CH₂—CH═N—O(n-C₄H₉) C₂H₅ Ia.2219 Cl CH₂—CH═N—O(n-C₄H₉) C₂H₅Ia.2220 H CH₂—CH═N—O(n-C₄H₉) n-C₃H₇ Ia.2221 F CH₂—CH═N—O(n-C₄H₉) n-C₃H₇Ia.2222 Cl CH₂—CH═N—O(n-C₄H₉) n-C₃H₇ Ia.2223 H CH₂—CH═N—O(n-C₄H₉) n-C₄H₉Ia.2224 F CH₂—CH═N—O(n-C₄H₉) n-C₄H₉ Ia.2225 Cl CH₂—CH═N—O(n-C₄H₉) n-C₄H₉Ia.2226 H CH₂—CH═N—O(n-C₄H₉) CH₂—CH═CH₂ Ia.2227 F CH₂—CH═N—O(n-C₄H₉)CH₂—CH═CH₂ Ia.2228 Cl CH₂—CH═N—O(n-C₄H₉) CH₂—CH═CH₂ Ia.2229 HCH₂—CH═N—O(n-C₄H₉) CH₂—C≡CH Ia.2230 F CH₂—CH═N—O(n-C₄H₉) CH₂—C≡CHIa.2231 Cl CH₂—CH═N—O(n-C₄H₉) CH₂—C≡CH Ia.2232 H CH₂—CH═N—O(n-C₄H₉)CH₂—CO—OCH₃ Ia.2233 F CH₂—CH═N—O(n-C₄H₉) CH₂—CO—OCH₃ Ia.2234 ClCH₂—CH═N—O(n-C₄H₉) CH₂—CO—OCH₃ Ia.2235 H CH₂—CH═N—O(n-C₄H₉) CH₂-phenylIa.2236 F CH₂—CH═N—O(n-C₄H₉) CH₂-phenyl Ia.2237 Cl CH₂—CH═N—O(n-C₄H₉)CH₂-phenyl Ia.2238 H CH₂—CH═N—OCH₂—CH═CH₂ CH₃ Ia.2239 FCH₂—CH═N—OCH₂—CH═CH₂ CH₃ Ia.2240 Cl CH₂—CH═N—OCH₂—CH═CH₂ CH₃ Ia.2241 HCH₂—CH═N—OCH₂—CH═CH₂ C₂H₅ Ia.2242 F CH₂—CH═N—OCH₂—CH═CH₂ C₂H₅ Ia.2243 ClCH₂—CH═N—OCH₂—CH═CH₂ C₂H₅ Ia.2244 H CH₂—CH═N—OCH₂—CH═CH₂ n-C₃H₇ Ia.2245F CH₂—CH═N—OCH₂—CH═CH₂ n-C₃H₇ Ia.2246 Cl CH₂—CH═N—OCH₂—CH═CH₂ n-C₃H₇Ia.2247 H CH₂—CH═N—OCH₂—CH═CH₂ n-C₄H₉ Ia.2248 F CH₂—CH═N—OCH₂—CH═CH₂n-C₄H₉ Ia.2249 Cl CH₂—CH═N—OCH₂—CH═CH₂ n-C₄H₉ Ia.2250 HCH₂—CH═N—OCH₂—CH═CH₂ CH₂—CH═CH₂ Ia.2251 F CH₂—CH═N—OCH₂—CH═CH₂CH₂—CH═CH₂ Ia.2252 Cl CH₂—CH═N—OCH₂—CH═CH₂ CH₂—CH═CH₂ Ia.2253 HCH₂—CH═N—OCH₂—CH═CH₂ CH₂—C≡CH Ia.2254 F CH₂—CH═N—OCH₂—CH═CH₂ CH₂—C≡CHIa.2255 Cl CH₂—CH═N—OCH₂—CH═CH₂ CH₂—C≡CH Ia.2256 H CH₂—CH═N—OCH₂—CH═CH₂CH₂—CO—OCH₃ Ia.2257 F CH₂—CH═N—OCH₂—CH═CH₂ CH₂—CO—OCH₃ Ia.2258 ClCH₂—CH═N—OCH₂—CH═CH₂ CH₂—CO—OCH₃ Ia.2259 H CH₂—CH═N—OCH₂—CH═CH₂CH₂-phenyl la.2260 F CH₂—CH═N—OCH₂—CH═CH₂ CH₂-phenyl Ia.2261 ClCH₂—CH═N—OCH₂—CH═CH₂ CH₂-phenyl Ia.2262 H CH₂—C(═N—OCH₃)—CO—OCH₃ CH₃Ia.2263 F CH₂—C(═N—OCH₃)—CO—OCH₃ CH₃ Ia.2264 Cl CH₂—C(═N—OCH₃)—CO—OCH₃CH₃ Ia.2265 H CH₂—C(═N—OCH₃)—CO—OCH₃ C₂H₅ Ia.2266 FCH₂—C(═N—OCH₃)—CO—OCH₃ C₂H₅ Ia.2267 Cl CH₂—C(═N—OCH₃)—CO—OCH₃ C₂H₅Ia.2268 H CH₂—C(═N—OCH₃)—CO—OCH₃ n-C₃H₇ Ia.2269 F CH₂—C(═N—OCH₃)—CO—OCH₃n-C₃H₇ Ia.2270 Cl CH₂—C(═N—OCH₃)—CO—OCH₃ n-C₃H₇ Ia.2271 HCH₂—C(═N—OCH₃)—CO—OCH₃ n-C₄H₉ Ia.2272 F CH₂—C(═N—OCH₃)—CO—OCH₃ n-C₄H₉Ia.2273 Cl CH₂—C(═N—OCH₃)—CO—OCH₃ n-C₄H₉ Ia.2274 HCH₂—C(═N—OCH₃)—CO—OCH₃ CH₂—CH═CH₂ Ia.2275 F CH₂—C(═N—OCH₃)—CO—OCH₃CH₂—CH═CH₂ Ia.2276 Cl CH₂—C(═N—OCH₃)—CO—OCH₃ CH₂—CH═CH₂ Ia.2277 HCH₂—C(═N—OCH₃)—CO—OCH₃ CH₂—C≡CH Ia.2278 F CH₂—C(═N—OCH₃)—CO—OCH₃CH₂—C≡CH Ia.2279 Cl CH₂—C(═N—OCH₃)—CO—OCH₃ CH₂—C≡CH Ia.2280 HCH₂—C(═N—OCH₃)—CO—OCH₃ CH₂—CO—OCH₃ Ia.2281 F CH₂—C(═N—OCH₃)—CO—OCH₃CH₂—CO—OCH₃ Ia.2282 Cl CH₂—C(═N—OCH₃)—CO—OCH₃ CH₂—CO—OCH₃ Ia.2283 HCH₂—C(═N—OCH₃)—CO—OCH₃ CH₂-phenyl Ia.2284 F CH₂—C(═N—OCH₃)—CO—OCH₃CH₂-phenyl Ia.2285 Cl CH₂—C(═N—OCH₃)—CO—OCH₃ CH₂-phenyl Ia.2286 HCH₂—COOH CH₃ Ia.2287 F CH₂—COOH CH₃ Ia.2288 Cl CH₂—COOH CH₃ Ia.2289 HCH₂—COOH C₂H₅ Ia.2290 F CH₂—COOH C₂H₅ Ia.2291 Cl CH₂—COOH C₂H₅ Ia.2292 HCH₂—COOH n-C₃H₇ Ia.2293 F CH₂—COOH n-C₃H₇ Ia.2294 Cl CH₂—COOH n-C₃H₇Ia.2295 H CH₂—COOH n-C₄H₉ Ia.2296 F CH₂—COOH n-C₄H₉ la.2297 Cl CH₂—COOHn-C₄H₉ Ia.2298 H CH₂—COOH CH₂—CH═CH₂ Ia.2299 F CH₂—COOH CH₂—CH═CH₂Ia.2300 Cl CH₂—COOH CH₂—CH═CH₂ Ia.2301 H CH₂—COOH CH₂—C≡CH la.2302 FCH₂—COOH CH₂—C≡CH Ia.2303 Cl CH₂—COOH CH₂—C≡CH Ia.2304 H CH₂—COOHCH₂—CO—OCH₃ Ia.2305 F CH₂—COOH CH₂—CO—OCH₃ Ia.2306 Cl CH₂—COOHCH₂—CO—OCH₃ Ia.2307 H CH₂—COOH CH₂-phenyl Ia.2308 F CH₂—COOH CH₂-phenylla.2309 Cl CH₂—COOH CH₂-phenyl Ia.2310 H CH(CH₃)—COOH CH₃ Ia.2311 FCH(CH₃)—COOH CH₃ Ia.2312 Cl CH(CH₃)—COOH CH₃ Ia.2313 H CH(CH₃)—COOH C₂H₅Ia.2314 F CH(CH₃)—COOH C₂H₅ Ia.2315 Cl CH(CH₃)—COOH C₂H₅ Ia.2316 HCH(CH₃)—COOH n-C₃H₇ Ia.2317 F CH(CH₃)—COOH n-C₃H₇ Ia.2318 ClCH(CH₃)—COOH n-C₃H₇ Ia.2319 H CH(CH₃)—COOH n-C₄H₉ Ia.2320 F CH(CH₃)—COOHn-C₄H₉ Ia.2321 Cl CH(CH₃)—COOH n-C₄H₉ Ia.2322 H CH(CH₃)—COOH CH₂—CH═CH₂Ia.2323 F CH(CH₃)—COOH CH₂—CH═CH₂ Ia.2324 Cl CH(CH₃)—COOH CH₂—CH═CH₂Ia.2325 H CH(CH₃)—COOH CH₂—C≡CH Ia.2326 F CH(CH₃)—COOH CH₂—C≡CH Ia.2327Cl CH(CH₃)—COOH CH₂—C≡CH Ia.2328 H CH(CH₃)—COOH CH₂—CO—OCH₃ Ia.2329 FCH(CH₃)—COOH CH₂—CO—OCH₃ Ia.2330 Cl CH(CH₃)—COOH CH₂—CO—OCH₃ Ia.2331 HCH(CH₃)—COOH CH₂-phenyl Ia.2332 F CH(CH₃)—COOH CH₂-phenyl Ia.2333 ClCH(CH₃)—COOH CH₂-phenyl Ia.2334 H CH(C₂H₅)—COOH CH₃ Ia.2335 FCH(C₂H₅)—COOH CH₃ Ia.2336 Cl CH(C₂H₅)—COOH CH₃ Ia.2337 H CH(C₂H₅)—COOHC₂H₅ Ia.2338 F CH(C₂H₅)—COOH C₂H₅ Ia.2339 Cl CH(C₂H₅)—COOH C₂H₅ Ia.2340H CH(C₂H₅)—COOH n-C₃H₇ Ia.2341 F CH(C₂H₅)—COOH n-C₃H₇ Ia.2342 ClCH(C₂H₅)—COOH n-C₃H₇ Ia 2343 H CH(C₂H₅)—COOH n-C₄H₉ Ia.2344 FCH(C₂H₅)—COOH n-C₄H₉ Ia.2345 Cl CH(C₂H₅)—COOH n-C₄H₉ Ia.2346 HCH(C₂H₅)—COOH CH₂—CH═CH₂ Ia.2347 F CH(C₂H₅)—COOH CH₂—CH═CH₂ Ia.2348 ClCH(C₂H₅)—COOH CH₂—CH═CH₂ Ia.2349 H CH(C₂H₅)—COOH CH₂—C≡CH Ia.2350 FCH(C₂H₅)—COOH CH₂—C≡CH Ia.2351 Cl CH(C₂H₅)—COOH CH₂—C≡CH Ia.2352 HCH(C₂H₅)—COOH CH₂—CO—OCH₃ Ia.2353 F CH(C₂H₅)—COOH CH₂—CO—OCH₃ Ia.2354 ClCH(C₂H₅)—COOH CH₂—CO—OCH₃ Ia.2355 H CH(C₂H₅)—COOH CH₂-phenyl Ia.2356 FCH(C₂H₅)—COOH CH₂-phenyl Ia.2357 Cl CH(C₂H₅)—COOH CH₂-phenyl Ia.2358 HCH₂—CO—OCH₃ CH₃ Ia.2359 F CH₂—CO—OCH₃ CH₃ Ia.2360 Cl CH₂—CO—OCH₃ CH₃Ia.2361 H CH₂—CO—OCH₃ C₂H₅ Ia.2362 F CH₂—CO—OCH₃ C₂H₅ Ia.2363 ClCH₂—CO—OCH₃ C₂H₅ Ia.2364 H CH₂—CO—OCH₃ n-C₃H₇ Ia.2365 F CH₂—CO—OCH₃n-C₃H₇ Ia.2366 Cl CH₂—CO—OCH₃ n-C₃H₇ Ia.2367 H CH₂—CO—OCH₃ n-C₄H₉Ia.2368 F CH₂—CO—OCH₃ n-C₄H₉ Ia.2369 Cl CH₂—CO—OCH₃ n-C₄H₉ Ia.2370 HCH₂—CO—OCH₃ CH₂—CH═CH₂ Ia.2371 F CH₂—CO—OCH₃ CH₂—CH═CH₂ Ia.2372 ClCH₂—CO—OCH₃ CH₂—CH═CH₂ Ia.2373 H CH₂—CO—OCH₃ CH₂—C≡CH Ia.2374 FCH₂—CO—OCH₃ CH₂—C≡CH Ia.2375 Cl CH₂—CO—OCH₃ CH₂—C≡CH Ia.2376 HCH₂—CO—OCH₃ CH₂—CO—OCH₃ Ia.2377 F CH₂—CO—OCH₃ CH₂—CO—OCH₃ Ia.2378 ClCH₂—CO—OCH₃ CH₂—CO—OCH₃ Ia.2379 H CH₂—CO—OCH₃ CH₂-phenyl Ia.2380 FCH₂—CO—OCH₃ CH₂-phenyl Ia.2381 Cl CH₂—CO—OCH₃ CH₂-phenyl Ia.2382 HCH(CH₃)—CO—OCH₃ CH₃ Ia.2383 F CH(CH₃)—CO—OCH₃ CH₃ Ia.2384 ClCH(CH₃)—CO—OCH₃ CH₃ Ia.2385 H CH(CH₃)—CO—OCH₃ C₂H₅ Ia.2386 FCH(CH₃)—CO—OCH₃ C₂H₅ Ia.2387 Cl CH(CH₃)—CO—OCH₃ C₂H₅ Ia.2388 HCH(CH₃)—CO—OCH₃ n-C₃H₇ Ia.2389 F CH(CH₃)—CO—OCH₃ n-C₃H₇ Ia.2390 ClCH(CH₃)—CO—OCH₃ n-C₃H₇ Ia.2391 H CH(CH₃)—CO—OCH₃ n-C₄H₉ Ia.2392 FCH(CH₃)—CO—OCH₃ n-C₄H₉ Ia.2393 Cl CH(CH₃)—CO—OCH₃ n-C₄H₉ Ia.2394 HCH(CH₃)—CO—OCH₃ CH₂—CH═CH₂ Ia.2395 F CH(CH₃)—CO—OCH₃ CH₂—CH═CH₂ Ia.2396Cl CH(CH₃)—CO—OCH₃ CH₂—CH═CH₂ Ia.2397 H CH(CH₃)—CO—OCH₃ CH₂—C≡CH Ia.2398F CH(CH₃)—CO—OCH₃ CH₂—C≡CH Ia.2399 Cl CH(CH₃)—CO—OCH₃ CH₂—C≡CH Ia.2400 HCH(CH₃)—CO—OCH₃ CH₂—CO—OCH₃ Ia.2401 F CH(CH₃)—CO—OCH₃ CH₂—CO—OCH₃Ia.2402 Cl CH(CH₃)—CO—OCH₃ CH₂—CO—OCH₃ Ia.2403 H CH(CH₃)—CO—OCH₃CH₂-phenyl Ia.2404 F CH(CH₃)—CO—OCH₃ CH₂-phenyl Ia.2405 ClCH(CH₃)—CO—OCH₃ CH₂-phenyl Ia.2406 H CH(C₂H₅)—CO—OCH₃ CH₃ Ia.2407 FCH(C₂H₅)—CO—OCH₃ CH₃ Ia.2408 Cl CH(C₂H₅)—CO—OCH₃ CH₃ Ia.2409 HCH(C₂H₅)—CO—OCH₃ C₂H₅ Ia.2410 F CH(C₂H₅)—CO—OCH₃ C₂H₅ Ia.2411 ClCH(C₂H₅)—CO—OCH₃ C₂H₅ Ia.2412 H CH(C₂H₅)—CO—OCH₃ n-C₃H₇ Ia.2413 FCH(C₂H₅)—CO—OCH₃ n-C₃H₇ Ia.2414 Cl CH(C₂H₅)—CO—OCH₃ n-C₃H₇ Ia.2415 HCH(C₂H₅)—CO—OCH₃ n-C₄H₉ Ia.2416 F CH(C₂H₅)—CO—OCH₃ n-C₄H₉ Ia.2417 ClCH(C₂H₅)—CO—OCH₃ n-C₄H₉ Ia.2418 H CH(C₂H₅)—CO—OCH₃ CH₂—CH═CH₂ Ia.2419 FCH(C₂H₅)—CO—OCH₃ CH₂—CH═CH₂ Ia.2420 Cl CH(C₂H₅)—CO—OCH₃ CH₂—CH═CH₂Ia.2421 H CH(C₂H₅)—CO—OCH₃ CH₂—C≡CH Ia.2422 F CH(C₂H₅)—CO—OCH₃ CH₂—C≡CHIa.2423 Cl CH(C₂H₅)—CO—OCH₃ CH₂—C≡CH Ia.2424 H CH(C₂H₅)—CO—OCH₃CH₂—CO—OCH₃ Ia.2425 F CH(C₂H₅)—CO—OCH₃ CH₂—CO—OCH₃ Ia.2426 ClCH(C₂H₅)—CO—OCH₃ CH₂—CO—OCH₃ la.2427 H CH(C₂H₅)—CO—OCH₃ CH₂-phenylIa.2428 F CH(C₂H₅)—CO—OCH₃ CH₂-phenyl Ia.2429 Cl CH(C₂H₅)—CO—OCH₃CH₂-phenyl Ia.2430 H CH₂—CO—OC₂H₅ CH₃ Ia.2431 F CH₂—CO—OC₂H₅ CH₃ Ia.2432Cl CH₂—CO—OC₂H₅ CH₃ Ia.2433 H CH₂—CO—OC₂H₅ C₂H₅ Ia.2434 F CH₂—CO—OC₂H₅C₂H₅ Ia.2435 Cl CH₂—CO—OC₂H₅ C₂H₅ Ia.2436 H CH₂—CO—OC₂H₅ n-C₃H₇ Ia.2437F CH₂—CO—OC₂H₅ n-C₃H₇ Ia.2438 Cl CH₂—CO—OC₂H₅ n-C₃H₇ Ia.2439 HCH₂—CO—OC₂H₅ n-C₄H₉ Ia.2440 F CH₂—CO—OC₂H₅ n-C₄H₉ Ia.2441 ClCH₂—CO—OC₂H₅ n-C₄H₉ Ia.2442 H CH₂—CO—OC₂H₅ CH₂—CH═CH₂ Ia.2443 FCH₂—CO—OC₂H₅ CH₂—CH═CH₂ Ia.2444 Cl CH₂—CO—OC₂H₅ CH₂—CH═CH₂ Ia.2445 HCH₂—CO—OC₂H₅ CH₂—C≡CH Ia.2446 F CH₂—CO—OC₂H₅ CH₂—C≡CH Ia.2447 ClCH₂—CO—OC₂H₅ CH₂—C≡CH Ia.2448 H CH₂—CO—OC₂H₅ CH₂—CO—OCH₃ Ia.2449 FCH₂—CO—OC₂H₅ CH₂—CO—OCH₃ Ia.2450 Cl CH₂—CO—OC₂H₅ CH₂—CO—OCH₃ Ia.2451 HCH₂—CO—OC₂H₅ CH₂-phenyl Ia.2452 F CH₂—CO—OC₂H₅ CH₂-phenyl Ia.2453 ClCH₂—CO—OC₂H₅ CH₂-phenyl Ia.2454 H CH(CH₃)—CO—OC₂H₅ CH₃ Ia.2455 FCH(CH₃)—CO—OC₂H₅ CH₃ Ia.2456 Cl CH(CH₃)—CO—OC₂H₅ CH₃ Ia.2457 HCH(CH₃)—CO—OC₂H₅ C₂H₅ Ia.2458 F CH(CH₃)—CO—OC₂H₅ C₂H₅ Ia.2459 ClCH(CH₃)—CO—OC₂H₅ C₂H₅ Ia.2460 H CH(CH₃)—CO—OC₂H₅ n-C₃H₇ Ia.2461 FCH(CH₃)—CO—OC₂H₅ n-C₃H₇ Ia.2462 Cl CH(CH₃)—CO—OC₂H₅ n-C₃H₇ Ia.2463 HCH(CH₃)—CO—OC₂H₅ n-C₄H₉ Ia.2464 F CH(CH₃)—CO—OC₂H₅ n-C₄H₉ Ia.2465 ClCH(CH₃)—CO—OC₂H₅ n-C₄H₉ Ia.2466 H CH(CH₃)—CO—OC₂H₅ CH₂—CH═CH₂ Ia.2467 FCH(CH₃)—CO—OC₂H₅ CH₂—CH═CH₂ Ia.2468 Cl CH(CH₃)—CO—OC₂H₅ CH₂—CH═CH₂Ia.2469 H CH(CH₃)—CO—OC₂H₅ CH₂—C≡CH Ia.2470 F CH(CH₃)—CO—OC₂H₅ CH₂—C≡CHIa.2471 Cl CH(CH₃)—CO—OC₂H₅ CH₂—C≡CH Ia.2472 H CH(CH₃)—CO—OC₂H₅CH₂—CO—OCH₃ Ia.2473 F CH(CH₃)—CO—OC₂H₅ CH₂—CO—OCH₃ Ia.2474 ClCH(CH₃)—CO—OC₂H₅ CH₂—CO—OCH₃ Ia.2475 H CH(CH₃)—CO—OC₂H₅ CH₂-phenylIa.2476 F CH(CH₃)—CO—OC₂H₅ CH₂-phenyl Ia.2477 Cl CH(CH₃)—CO—OC₂H₅CH₂-phenyl Ia.2478 H CH(C₂H₅)—CO—OC₂H₅ CH₃ Ia.2479 F CH(C₂H₅)—CO—OC₂H₅CH₃ Ia.2480 Cl CH(C₂H₅)—CO—OC₂H₅ CH₃ Ia.2481 H CH(C₂H₅)—CO—OC₂H₅ C₂H₅Ia.2482 F CH(C₂H₅)—CO—OC₂H₅ C₂H₅ Ia.2483 Cl CH(C₂H₅)—CO—OC₂H₅ C₂H₅Ia.2484 H CH(C₂H₅)—CO—OC₂H₅ n-C₃H₇ Ia.2485 F CH(C₂H₅)—CO—OC₂H₅ n-C₃H₇Ia.2486 Cl CH(C₂H₅)—CO—OC₂H₅ n-C₃H₇ Ia.2487 H CH(C₂H₅)—CO—OC₂H₅ n-C₄H₉Ia.2488 F CH(C₂H₅)—CO—OC₂H₅ n-C₄H₉ Ia.2489 Cl CH(C₂H₅)—CO—OC₂H₅ n-C₄H₉Ia.2490 H CH(C₂H₅)—CO—OC₂H₅ CH₂—CH═CH₂ Ia.2491 F CH(C₂H₅)—CO—OC₂H₅CH₂—CH═CH₂ Ia.2492 Cl CH(C₂H₅)—CO—OC₂H₅ CH₂—CH═CH₂ Ia.2493 HCH(C₂H₅)—CO—OC₂H₅ CH₂—C≡CH Ia.2494 F CH(C₂H₅)—CO—OC₂H₅ CH₂—C≡CH Ia.2495Cl CH(C₂H₅)—CO—OC₂H₅ CH₂—C≡CH Ia.2496 H CH(C₂H₅)—CO—OC₂H₅ CH₂—CO—OCH₃Ia.2497 F CH(C₂H₅)—CO—OC₂H₅ CH₂—CO—OCH₃ Ia.2498 Cl CH(C₂H₅)—CO—OC₂H₅CH₂—CO—OCH₃ Ia.2499 H CH(C₂H₅)—CO—OC₂H₅ CH₂-phenyl Ia.2500 FCH(C₂H₅)—CO—OC₂H₅ CH₂-phenyl Ia.2501 Cl CH(C₂H₅)—CO—OC₂H₅ CH₂-phenylIa.2502 H CH₂—CO—OC(CH₃)₃ CH₃ Ia.2503 F CH₂—CO—OC(CH₃)₃ CH₃ Ia.2504 ClCH₂—CO—OC(CH₃)₃ CH₃ Ia.2505 H CH₂—CO—OC(CH₃)₃ C₂H₅ Ia.2506 FCH₂—CO—OC(CH₃)₃ C₂H₅ Ia.2507 Cl CH₂—CO—OC(CH₃)₃ C₂H₅ Ia.2508 HCH₂—CO—OC(CH₃)₃ n-C₃H₇ Ia.2509 F CH₂—CO—OC(CH₃)₃ n-C₃H₇ Ia.2510 ClCH₂—CO—OC(CH₃)₃ n-C₃H₇ Ia.2511 H CH₂—CO—OC(CH₃)₃ n-C₄H₉ Ia.2512 FCH₂—CO—OC(CH₃)₃ n-C₄H₉ Ia.2513 Cl CH₂—CO—OC(CH₃)₃ n-C₄H₉ Ia.2514 HCH₂—CO—OC(CH₃)₃ CH₂—CH═CH₂ Ia.2515 F CH₂—CO—OC(CH₃)₃ CH₂—CH═CH₂ Ia.2516Cl CH₂—CO—OC(CH₃)₃ CH₂—CH═CH₂ Ia.2517 H CH₂—CO—OC(CH₃)₃ CH₂—C≡CH Ia.2518F CH₂—CO—OC(CH₃)₃ CH₂—C≡CH Ia.2519 Cl CH₂—CO—OC(CH₃)₃ CH₂—C≡CH Ia.2520 HCH₂—CO—OC(CH₃)₃ CH₂—CO—OCH₃ Ia.2521 F CH₂—CO—OC(CH₃)₃ CH₂—CO—OCH₃Ia.2522 Cl CH₂—CO—OC(CH₃)₃ CH₂—CO—OCH₃ Ia.2523 H CH₂—CO—OC(CH₃)₃CH₂-phenyl Ia.2524 F CH₂—CO—OC(CH₃)₃ CH₂-phenyl Ia.2525 ClCH₂—CO—OC(CH₃)₃ CH₂-phenyl Ia.2526 H CH(CH₃)—CO—OC(CH₃)₃ CH₃ Ia.2527 FCH(CH₃)—CO—OC(CH₃)₃ CH₃ Ia.2528 Cl CH(CH₃)—CO—OC(CH₃)₃ CH₃ Ia.2529 HCH(CH₃)—CO—OC(CH₃)₃ C₂H₅ Ia.2530 F CH(CH₃)—CO—OC(CH₃)₃ C₂H₅ Ia.2531 ClCH(CH₃)—CO—OC(CH₃)₃ C₂H₅ Ia.2532 H CH(CH₃)—CO—OC(CH₃)₃ n-C₃H₇ Ia.2533 FCH(CH₃)—CO—OC(CH₃)₃ n-C₃H₇ Ia.2534 Cl CH(CH₃)—CO—OC(CH₃)₃ n-C₃H₇ Ia.2535H CH(CH₃)—CO—OC(CH₃)₃ n-C₄H₉ Ia.2536 F CH(CH₃)—CO—OC(CH₃)₃ n-C₄H₉Ia.2537 Cl CH(CH₃)—CO—OC(CH₃)₃ n-C₄H₉ Ia.2538 H CH(CH₃)—CO—OC(CH₃)₃CH₂—CH═CH₂ Ia.2539 F CH(CH₃)—CO—OC(CH₃)₃ CH₂—CH═CH₂ Ia.2540 ClCH(CH₃)—CO—OC(CH₃)₃ CH₂—CH═CH₂ Ia.2541 H CH(CH₃)—CO—OC(CH₃)₃ CH₂—C≡CHIa.2542 F CH(CH₃)—CO—OC(CH₃)₃ CH₂—C≡CH Ia.2543 Cl CH(CH₃)—CO—OC(CH₃)₃CH₂—C≡CH Ia.2544 H CH(CH₃)—CO—OC(CH₃)₃ CH₂—CO—OCH₃ Ia.2545 FCH(CH₃)—CO—OC(CH₃)₃ CH₂—CO—OCH₃ Ia.2546 Cl CH(CH₃)—CO—OC(CH₃)₃CH₂—CO—OCH₃ Ia.2547 H CH(CH₃)—CO—OC(CH₃)₃ CH₂-phenyl Ia.2548 FCH(CH₃)—CO—OC(CH₃)₃ CH₂-phenyl Ia.2549 Cl CH(CH₃)—CO—OC(CH₃)₃ CH₂-phenylIa.2550 H CH(C₂H₅)—CO—OC(CH₃)₃ CH₃ Ia.2551 F CH(C₂H₅)—CO—OC(CH₃)₃ CH₃Ia.2552 Cl CH(C₂H₅)—CO—OC(CH₃)₃ CH₃ Ia.2553 H CH(C₂H₅)—CO—OC(CH₃)₃ C₂H₅Ia.2554 F CH(C₂H₅)—CO—OC(CH₃)₃ C₂H₅ Ia.2555 Cl CH(C₂H₅)—CO—OC(CH₃)₃ C₂H₅Ia.2556 H CH(C₂H₅)—CO—OC(CH₃)₃ n-C₃H₇ Ia.2557 F CH(C₂H₅)—CO—OC(CH₃)₃n-C₃H₇ Ia.2558 Cl CH(C₂H₅)—CO—OC(CH₃)₃ n-C₃H₇ Ia.2559 HCH(C₂H₅)—CO—OC(CH₃)₃ n-C₄H₉ Ia.2560 F CH(C₂H₅)—CO—OC(CH₃)₃ n-C₄H₉Ia.2561 Cl CH(C₂H₅)—CO—OC(CH₃)₃ n-C₄H₉ Ia.2562 H CH(C₂H₅)—CO—OC(CH₃)₃CH₂—CH═CH₂ Ia.2563 F CH(C₂H₅)—CO—OC(CH₃)₃ CH₂—CH═CH₂ Ia.2564 ClCH(C₂H₅)—CO—OC(CH₃)₃ CH₂—CH═CH₂ Ia.2565 H CH(C₂H₅)—CO—OC(CH₃)₃ CH₂—C≡CHIa.2566 F CH(C₂H₅)—CO—OC(CH₃)₃ CH₂—C═CH Ia.2567 Cl CH(C₂H₅)—CO—OC(CH₃)₃CH₂—C≡CH Ia.2568 H CH(C₂H₅)—CO—OC(CH₃)₃ CH₂—CO—OCH₃ Ia.2569 FCH(C₂H₅)—CO—OC(CH₃)₃ CH₂—CO—OCH₃ Ia.2570 Cl CH(C₂H₅)—CO—OC(CH₃)₃CH₂—CO—OCH₃ Ia.2571 H CH(C₂H₅)—CO—OC(CH₃)₃ CH₂-phenyl Ia.2572 FCH(C₂H₅)—CO—OC(CH₃)₃ CH₂-phenyl Ia.2573 Cl CH(C₂H₅)—CO—OC(CH₃)₃CH₂-phenyl Ia.2574 H CH₂—CO—SCH₃ CH₃ Ia.2575 F CH₂—CO—SCH₃ CH₃ Ia.2576Cl CH₂—CO—SCH₃ CH₃ Ia.2577 H CH₂—CO—SCH₃ C₂H₅ Ia.2578 F CH₂—CO—SCH₃ C₂H₅Ia.2579 Cl CH₂—CO—SCH₃ C₂H₅ Ia.2580 H CH₂—CO—SCH₃ n-C₃H₇ Ia.2581 FCH₂—CO—SCH₃ n-C₃H₇ Ia.2582 Cl CH₂—CO—SCH₃ n-C₃H₇ Ia.2583 H CH₂—CO—SCH₃n-C₄H₉ Ia.2584 F CH₂—CO—SCH₃ n-C₄H₉ Ia.2585 Cl CH₂—CO—SCH₃ n-C₄H₉Ia.2586 H CH₂—CO—SCH₃ CH₂—CH═CH₂ Ia.2587 F CH₂—CO—SCH₃ CH₂—CH═CH₂Ia.2588 Cl CH₂—CO—SCH₃ CH₂—CH═CH₂ Ia.2589 H CH₂—CO—SCH₃ CH₂—C≡CH Ia.2590F CH₂—CO—SCH₃ CH₂—C≡CH Ia.2591 Cl CH₂—CO—SCH₃ CH₂—C≡CH Ia.2592 HCH₂—CO—SCH₃ CH₂—CO—OCH₃ Ia.2593 F CH₂—CO—SCH₃ CH₂—CO—OCH₃ Ia.2594 ClCH₂—CO—SCH₃ CH₂—CO—OCH₃ Ia.2595 H CH₂—CO—SCH₃ CH₂-phenyl Ia.2596 FCH₂—CO—SCH₃ CH₂-phenyl Ia.2597 Cl CH₂—CO—SCH₃ CH₂-phenyl Ia.2598 HCH₂—CO—NH₂ CH₃ Ia.2599 F CH₂—CO—NH₂ CH₃ Ia.2600 Cl CH₂—CO—NH₂ CH₃Ia.2601 H CH₂—CO—NH₂ C₂H₅ Ia.2602 F CH₂—CO—NH₂ C₂H₅ Ia.2603 ClCH₂—CO—NH₂ C₂H₅ Ia.2604 H CH₂—CO—NH₂ n-C₃H₇ Ia.2605 F CH₂—CO—NH₂ n-C₃H₇Ia.2606 Cl CH₂—CO—NH₂ n-C₃H₇ Ia.2607 H CH₂—CO—NH₂ n-C₄H₉ Ia.2608 FCH₂—CO—NH₂ n-C₄H₉ Ia.2609 Cl CH₂—CO—NH₂ n-C₄H₉ Ia.2610 H CH₂—CO—NH₂CH₂—CH═CH₂ Ia.2611 F CH₂—CO—NH₂ CH₂—CH═CH₂ Ia.2612 Cl CH₂—CO—NH₂CH₂—CH═CH₂ Ia.2613 H CH₂—CO—NH₂ CH₂—C≡CH Ia.2614 F CH₂—CO—NH₂ CH₂—C≡CHIa.2615 Cl CH₂—CO—NH₂ CH₂—C≡CH Ia.2616 H CH₂—CO—NH₂ CH₂—CO—OCH₃ Ia.2617F CH₂—CO—NH₂ CH₂—CO—OCH₃ Ia.2618 Cl CH₂—CO—NH₂ CH₂—CO—OCH₃ Ia.2619 HCH₂—CO—NH₂ CH₂-phenyl Ia.2620 F CH₂—CO—NH₂ CH₂-phenyl Ia.2621 ClCH₂—CO—NH₂ CH₂-phenyl Ia.2622 H CH(CH₃)—CO—NH₂ CH₃ Ia.2623 FCH(CH₃)—CO—NH₂ CH₃ Ia.2624 Cl CH(CH₃)—CO—NH₂ CH₃ Ia.2625 HCH(CH₃)—CO—NH₂ C₂H₅ Ia.2626 F CH(CH₃)—CO—NH₂ C₂H₅ Ia.2627 ClCH(CH₃)—CO—NH₂ C₂H₅ Ia.2628 H CH(CH₃)—CO—NH₂ n-C₃H₇ Ia.2629 FCH(CH₃)—CO—NH₂ n-C₃H₇ Ia.2630 Cl CH(CH₃)—CO—NH₂ n-C₃H₇ Ia.2631 HCH(CH₃)—CO—NH₂ n-C₄H₉ Ia.2632 F CH(CH₃)—CO—NH₂ n-C₄H₉ Ia.2633 ClCH(CH₃)—CO—NH₂ n-C₄H₉ Ia.2634 H CH(CH₃)—CO—NH₂ CH₂—CH═CH₂ Ia.2635 FCH(CH₃)—CO—NH₂ CH₂—CH═CH₂ Ia.2636 Cl CH(CH₃)—CO—NH₂ CH₂—CH═CH₂ Ia.2637 HCH(CH₃)—CO—NH₂ CH₂—C≡CH Ia.2638 F CH(CH₃)—CO—NH₂ CH₂—C≡CH Ia.2639 ClCH(CH₃)—CO—NH₂ CH₂—C≡CH Ia.2640 H CH(CH₃)—CO—NH₂ CH₂—CO—OCH₃ Ia.2641 FCH(CH₃)—CO—NH₂ CH₂—CO—OCH₃ Ia.2642 Cl CH(CH₃)—CO—NH₂ CH₂—CO—OCH₃ Ia.2643H CH(CH₃)—CO—NH₂ CH₂-phenyl Ia.2644 F CH(CH₃)—CO—NH₂ CH₂-phenyl Ia.2645Cl CH(CH₃)—CO—NH₂ CH₂-phenyl Ia.2646 H CH(C₂H₅)—CO—NH₂ CH₃ Ia.2647 FCH(C₂H₅)—CO—NH₂ CH₃ Ia.2648 Cl CH(C₂H₅)—CO—NH₂ CH₃ Ia.2649 HCH(C₂H₅)—CO—NH₂ C₂H₅ Ia.2650 F CH(C₂H₅)—CO—NH₂ C₂H₅ Ia.2651 ClCH(C₂H₅)—CO—NH₂ C₂H₅ Ia.2652 H CH(C₂H₅)—CO—NH₂ n-C₃H₇ Ia.2653 FCH(C₂H₅)—CO—NH₂ n-C₃H₇ Ia.2654 Cl CH(C₂H₅)—CO—NH₂ n-C₃H₇ Ia.2655 HCH(C₂H₅)—CO—NH₂ n-C₄H₉ Ia.2656 F CH(C₂H₅)—CO—NH₂ n-C₄H₉ Ia.2657 ClCH(C₂H₅)—CO—NH₂ n-C₄H₉ Ia.2658 H CH(C₂H₅)—CO—NH₂ CH₂—CH═CH₂ Ia.2659 FCH(C₂H₅)—CO—NH₂ CH₂—CH═CH₂ Ia.2660 Cl CH(C₂H₅)—CO—NH₂ CH₂—CH═CH₂ Ia.2661H CH(C₂H₅)—CO—NH₂ CH₂—C≡CH Ia.2662 F CH(C₂H₅)—CO—NH₂ CH₂—C≡CH Ia.2663 ClCH(C₂H₅)—CO—NH₂ CH₂—C≡CH Ia.2664 H CH(C₂H₅)—CO—NH₂ CH₂—CO—OCH₃ Ia.2665 FCH(C₂H₅)—CO—NH₂ CH₂—CO—OCH₃ Ia.2666 Cl CH(C₂H₅)—CO—NH₂ CH₂—CO—OCH₃Ia.2667 H CH(C₂H₅)—CO—NH₂ CH₂-phenyl Ia.2668 F CH(C₂H₅)—CO—NH₂CH₂-phenyl Ia.2669 Cl CH(C₂H₅)—CO—NH₂ CH₂-phenyl Ia.2670 H CH₂—CO—NH—CH₃CH₃ Ia.2671 F CH₂—CO—NH—CH₃ CH₃ Ia.2672 Cl CH₂—CO—NH—CH₃ CH₃ Ia.2673 HCH₂—CO—NH—CH₃ C₂H₅ Ia.2674 F CH₂—CO—NH—CH₃ C₂H₅ Ia.2675 Cl CH₂—CO—NH—CH₃C₂H₅ Ia.2676 H CH₂—CO—NH—CH₃ n-C₃H₇ Ia.2677 F CH₂—CO—NH—CH₃ n-C₃H₇Ia.2678 Cl CH₂—CO—NH—CH₃ n-C₃H₇ Ia.2679 H CH₂—CO—NH—CH₃ n-C₄H₉ Ia.2680 FCH₂—CO—NH—CH₃ n-C₄H₉ Ia.2681 Cl CH₂—CO—NH—CH₃ n-C₄H₉ Ia.2682 HCH₂—CO—NH—CH₃ CH₂—CH═CH₂ Ia.2683 F CH₂—CO—NH—CH₃ CH₂—CH═CH₂ Ia.2684 ClCH₂—CO—NH—CH₃ CH₂—CH═CH₂ Ia.2685 H CH₂—CO—NH—CH₃ CH₂—C≡CH Ia.2686 FCH₂—CO—NH—CH₃ CH₂—C≡CH Ia.2687 Cl CH₂—CO—NH—CH₃ CH₂—C≡CH Ia.2688 HCH₂—CO—NH—CH₃ CH₂—CO—OCH₃ Ia.2689 F CH₂—CO—NH—CH₃ CH₂—CO—OCH₃ Ia.2690 ClCH₂—CO—NH—CH₃ CH₂—CO—OCH₃ Ia.2691 H CH₂—CO—NH—CH₃ CH₂-phenyl Ia.2692 FCH₂—CO—NH—CH₃ CH₂-phenyl Ia.2693 Cl CH₂—CO—NH—CH₃ CH₂-phenyl Ia.2694 HCH(CH₃)—CO—NH—CH₃ CH₃ Ia.2695 F CH(CH₃)—CO—NH—CH₃ CH₃ Ia.2696 ClCH(CH₃)—CO—NH—CH₃ CH₃ Ia.2697 H CH(CH₃)—CO—NH—CH₃ C₂H₅ Ia.2698 FCH(CH₃)—CO—NH—CH₃ C₂H₅ Ia.2699 Cl CH(CH₃)—CO—NH—CH₃ C₂H₅ Ia.2700 HCH(CH₃)—CO—NH—CH₃ n-C₃H₇ Ia.2701 F CH(CH₃)—CO—NH—CH₃ n-C₃H₇ Ia.2702 ClCH(CH₃)—CO—NH—CH₃ n-C₃H₇ Ia.2703 H CH(CH₃)—CO—NH—CH₃ n-C₄H₉ Ia.2704 FCH(CH₃)—CO—NH—CH₃ n-C₄H₉ Ia.2705 Cl CH(CH₃)—CO—NH—CH₃ n-C₄H₉ Ia.2706 HCH(CH₃)—CO—NH—CH₃ CH₂—CH═CH₂ Ia.2707 F CH(CH₃)—CO—NH—CH₃ CH₂—CH═CH₂Ia.2708 Cl CH(CH₃)—CO—NH—CH₃ CH₂—CH═CH₂ Ia.2709 H CH(CH₃)—CO—NH—CH₃CH₂—C≡CH Ia.2710 F CH(CH₃)—CO—NH—CH₃ CH₂—C≡CH Ia.2711 ClCH(CH₃)—CO—NH—CH₃ CH₂—C≡CH Ia.2712 H CH(CH₃)—CO—NH—CH₃ CH₂—CO—OCH₃Ia.2713 F CH(CH₃)—CO—NH—CH₃ CH₂—CO—OCH₃ Ia.2714 Cl CH(CH₃)—CO—NH—CH₃CH₂—CO—OCH₃ Ia.2715 H CH(CH₃)—CO—NH—CH₃ CH₂-phenyl Ia.2716 FCH(CH₃)—CO—NH—CH₃ CH₂-phenyl Ia.2717 Cl CH(CH₃)—CO—NH—CH₃ CH₂-phenylIa.2718 H CH(C₂H₅)—CO—NH—CH₃ CH₃ Ia.2719 F CH(C₂H₅)—CO—NH—CH₃ CH₃Ia.2720 Cl CH(C₂H₅)—CO—NH—CH₃ CH₃ Ia.2721 H CH(C₂H₅)—CO—NH—CH₃ C₂H₅Ia.2722 F CH(C₂H₅)—CO—NH—CH₃ C₂H₅ Ia.2723 Cl CH(C₂H₅)—CO—NH—CH₃ C₂H₅Ia.2724 H CH(C₂H₅)—CO—NH—CH₃ n-C₃H₇ Ia.2725 F CH(C₂H₅)—CO—NH—CH₃ n-C₃H₇Ia.2726 Cl CH(C₂H₅)—CO—NH—CH₃ n-C₃H₇ Ia.2727 H CH(C₂H₅)—CO—NH—CH₃ n-C₄H₉Ia.2728 F CH(C₂H₅)—CO—NH—CH₃ n-C₄H₉ Ia.2729 Cl CH(C₂H₅)—CO—NH—CH₃ n-C₄H₉Ia.2730 H CH(C₂H₅)—CO—NH—CH₃ CH₂—CH═CH₂ Ia.2731 F CH(C₂H₅)—CO—NH—CH₃CH₂—CH═CH₂ Ia.2732 Cl CH(C₂H₅)—CO—NH—CH₃ CH₂—CH═CH₂ Ia.2733 HCH(C₂H₅)—CO—NH—CH₃ CH₂—C≡CH Ia.2734 F CH(C₂H₅)—CO—NH—CH₃ CH₂—C≡CHIa.2735 Cl CH(C₂H₅)—CO—NH—CH₃ CH₂—C≡CH Ia.2736 H CH(C₂H₅)—CO—NH—CH₃CH₂—CO—OCH₃ Ia.2737 F CH(C₂H₅)—CO—NH—CH₃ CH₂—CO—OCH₃ Ia.2738 ClCH(C₂H₅)—CO—NH—CH₃ CH₂—CO—OCH₃ Ia.2739 H CH(C₂H₅)—CO—NH—CH₃ CH₂-phenylIa.2740 F CH(C₂H₅)—CO—NH—CH₃ CH₂-phenyl Ia.2741 Cl CH(C₂H₅)—CO—NH—CH₃CH₂-phenyl Ia.2742 H CH₂—CO—N(CH₃)₂ CH₃ Ia.2743 F CH₂—CO—N(CH₃)₂ CH₃Ia.2744 Cl CH₂—CO—N(CH₃)₂ CH₃ Ia.2745 H CH₂—CO—N(CH₃)₂ C₂H₅ Ia.2746 FCH₂—CO—N(CH₃)₂ C₂H₅ Ia.2747 Cl CH₂—CO—N(CH₃)₂ C₂H₅ Ia.2748 HCH₂—CO—N(CH₃)₂ n-C₃H₇ Ia.2749 F CH₂—CO—N(CH₃)₂ n-C₃H₇ Ia.2750 ClCH₂—CO—N(CH₃)₂ n-C₃H₇ Ia.2751 H CH₂—CO—N(CH₃)₂ n-C₄H₉ Ia.2752 FCH₂—CO—N(CH₃)₂ n-C₄H₉ Ia.2753 Cl CH₂—CO—N(CH₃)₂ n-C₄H₉ Ia.2754 HCH₂—CO—N(CH₃)₂ CH₂—CH═CH₂ Ia.2755 F CH₂—CO—N(CH₃)₂ CH₂—CH═CH₂ Ia.2756 ClCH₂—CO—N(CH₃)₂ CH₂—CH═CH₂ Ia.2757 H CH₂—CO—N(CH₃)₂ CH₂—C≡CH Ia.2758 FCH₂—CO—N(CH₃)₂ CH₂—C≡CH Ia.2759 Cl CH₂—CO—N(CH₃)₂ CH₂—C≡CH Ia.2760 HCH₂—CO—N(CH₃)₂ CH₂—CO—OCH₃ Ia.2761 F CH₂—CO—N(CH₃)₂ CH₂—CO—OCH₃ Ia.2762Cl CH₂—CO—N(CH₃)₂ CH₂—CO—OCH₃ Ia.2763 H CH₂—CO—N(CH₃)₂ CH₂-phenylIa.2764 F CH₂—CO—N(CH₃)₂ CH₂-phenyl Ia.2765 Cl CH₂—CO—N(CH₃)₂ CH₂-phenylIa.2766 H CH(CH₃)—CO—N(CH₃)₂ CH₃ Ia.2767 F CH(CH₃)—CO—N(CH₃)₂ CH₃Ia.2768 Cl CH(CH₃)—CO—N(CH₃)₂ CH₃ Ia.2769 H CH(CH₃)—CO—N(CH₃)₂ C₂H₅Ia.2770 F CH(CH₃)—CO—N(CH₃)₂ C₂H₅ Ia.2771 Cl CH(CH₃)—CO—N(CH₃)₂ C₂H₅Ia.2772 H CH(CH₃)—CO—N(CH₃)₂ n-C₃H₇ Ia.2773 F CH(CH₃)—CO—N(CH₃)₂ n-C₃H₇Ia.2774 Cl CH(CH₃)—CO—N(CH₃)₂ n-C₃H₇ Ia.2775 H CH(CH₃)—CO—N(CH₃)₂ n-C₄H₉Ia.2776 F CH(CH₃)—CO—N(CH₃)₂ n-C₄H₉ Ia.2777 Cl CH(CH₃)—CO—N(CH₃)₂ n-C₄H₉Ia.2778 H CH(CH₃)—CO—N(CH₃)₂ CH₂—CH═CH₂ Ia.2779 F CH(CH₃)—CO—N(CH₃)₂CH₂—CH═CH₂ Ia.2780 Cl CH(CH₃)—CO—N(CH₃)₂ CH₂—CH═CH₂ Ia.2781 HCH(CH₃)—CO—N(CH₃)₂ CH₂—C≡CH Ia.2782 F CH(CH₃)—CO—N(CH₃)₂ CH₂—C≡CHIa.2783 Cl CH(CH₃)—CO—N(CH₃)₂ CH₂—C≡CH Ia.2784 H CH(CH₃)—CO—N(CH₃)₂CH₂—CO—OCH₃ Ia.2785 F CH(CH₃)—CO—N(CH₃)₂ CH₂—CO—OCH₃ Ia.2786 ClCH(CH₃)—CO—N(CH₃)₂ CH₂—CO—OCH₃ Ia.2787 H CH(CH₃)—CO—N(CH₃)₂ CH₂-phenylIa.2788 F CH(CH₃)—CO—N(CH₃)₂ CH₂-phenyl Ia.2789 Cl CH(CH₃)—CO—N(CH₃)₂CH₂-phenyl Ia.2790 H CH(C₂H₅)—CO—N(CH₃)₂ CH₃ Ia.2791 FCH(C₂H₅)—CO—N(CH₃)₂ CH₃ Ia.2792 Cl CH(C₂H₅)—CO—N(CH₃)₂ CH₃ Ia.2793 HCH(C₂H₅)—CO—N(CH₃)₂ C₂H₅ Ia.2794 F CH(C₂H₅)—CO—N(CH₃)₂ C₂H₅ Ia.2795 ClCH(C₂H₅)—CO—N(CH₃)₂ C₂H₅ Ia.2796 H CH(C₂H₅)—CO—N(CH₃)₂ n-C₃H₇ Ia.2797 FCH(C₂H₅)—CO—N(CH₃)₂ n-C₃H₇ Ia.2798 Cl CH(C₂H₅)—CO—N(CH₃)₂ n-C₃H₇ Ia.2799H CH(C₂H₅)—CO—N(CH₃)₂ n-C₄H₉ Ia.2800 F CH(C₂H₅)—CO—N(CH₃)₂ n-C₄H₉Ia.2801 Cl CH(C₂H₅)—CO—N(CH₃)₂ n-C₄H₉ Ia.2802 H CH(C₂H₅)—CO—N(CH₃)₂CH₂—CH═CH₂ Ia.2803 F CH(C₂H₅)—CO—N(CH₃)₂ CH₂—CH═CH₂ Ia.2804 ClCH(C₂H₅)—CO—N(CH₃)₂ CH₂—CH═CH₂ Ia.2805 H CH(C₂H₅)—CO—N(CH₃)₂ CH₂—C≡CHIa.2806 F CH(C₂H₅)—CO—N(CH₃)₂ CH₂—C≡CH Ia.2807 Cl CH(C₂H₅)—CO—N(CH₃)₂CH₂—C≡CH Ia.2808 H CH(C₂H₅)—CO—N(CH₃)₂ CH₂—CO—OCH₃ Ia.2809 FCH(C₂H₅)—CO—N(CH₃)₂ CH₂—CO—OCH₃ Ia.2810 Cl CH(C₂H₅)—CO—N(CH₃)₂CH₂—CO—OCH₃ Ia.2811 H CH(C₂H₅)—CO—N(CH₃)₂ CH₂-phenyl Ia.2812 FCH(C₂H₅)—CO—N(CH₃)₂ CH₂-phenyl Ia.2813 Cl CH(C₂H₅)—CO—N(CH₃)₂ CH₂-phenylIa.2814 H cyclopentyl CH₃ Ia.2815 F cyclopentyl CH₃ Ia.2816 Clcyclopentyl CH₃ Ia.2817 H cyclopentyl C₂H₅ Ia.2818 F cyclopentyl C₂H₅Ia.2819 Cl cyclopentyl C₂H₅ Ia.2820 H cyclopentyl n-C₃H₇ Ia.2821 Fcyclopentyl n-C₃H₇ Ia.2822 Cl cyclopentyl n-C₃H₇ Ia.2823 H cyclopentyln-C₄H₉ Ia.2824 F cyclopentyl n-C₄H₉ Ia.2825 Cl cyclopentyl n-C₄H₉Ia.2826 H cyclopentyl CH₂—CH═CH₂ Ia.2827 F cyclopentyl CH₂—CH═CH₂Ia.2828 Cl cyclopentyl CH₂—CH═CH₂ Ia.2829 H cyclopentyl CH₂—C≡CH Ia.2830F cyclopentyl CH₂—C≡CH Ia.2831 Cl cyclopentyl CH₂—C≡CH Ia.2832 Hcyclopentyl CH₂—CO—OCH₃ Ia.2833 F cyclopentyl CH₂—CO—OCH₃ Ia.2834 Clcyclopentyl CH₂—CO—OCH₃ Ia.2835 H cyclopentyl CH₂-phenyl Ia.2836 Fcyclopentyl CH₂-phenyl Ia.2837 Cl cyclopentyl CH₂-phenyl Ia.2838 Hcyclohexyl CH₃ Ia.2839 F cyclohexyl CH₃ Ia.2840 Cl cyclohexyl CH₃Ia.2841 H cyclohexyl C₂H₅ Ia.2842 F cyclohexyl C₂H₅ Ia.2843 Clcyclohexyl C₂H₅ Ia.2844 H cyclohexyl n-C₃H₇ Ia.2845 F cyclohexyl n-C₃H₇Ia.2846 Cl cyclohexyl n-C₃H₇ Ia.2847 H cyclohexyl n-C₄H₉ Ia.2848 Fcyclohexyl n-C₄H₉ Ia.2849 Cl cyclohexyl n-C₄H₉ Ia.2850 H cyclohexylCH₂—CH═CH₂ Ia.2851 F cyclohexyl CH₂—CH═CH₂ Ia.2852 Cl cyclohexylCH₂—CH═CH₂ Ia.2853 H cyclohexyl CH₂—C≡CH Ia.2854 F cyclohexyl CH₂—C≡CHIa.2855 Cl cyclohexyl CH₂—C≡CH Ia.2856 H cyclohexyl CH₂—CO—OCH₃ Ia.2857F cyclohexyl CH₂—CO—OCH₃ Ia.2858 Cl cyclohexyl CH₂—CO—OCH₃ Ia.2859 Hcyclohexyl CH₂-phenyl Ia.2860 F cyclohexyl CH₂-phenyl Ia.2861 Clcyclohexyl CH₂-phenyl Ia.2862 H CH₂-cyclopentyl CH₃ Ia.2863 FCH₂-cyclopentyl CH₃ Ia.2864 Cl CH₂-cyclopentyl CH₃ Ia.2865 HCH₂-cyclopentyl C₂H₅ Ia.2866 F CH₂-cyclopentyl C₂H₅ Ia.2867 ClCH₂-cyclopentyl C₂H₅ Ia.2868 H CH₂-cyclopentyl n-C₃H₇ Ia.2869 FCH₂-cyclopentyl n-C₃H₇ Ia.2870 Cl CH₂-cyclopentyl n-C₃H₇ Ia.2871 HCH₂-cyclopentyl n-C₄H₉ Ia.2872 F CH₂-cyclopentyl n-C₄H₉ Ia.2873 ClCH₂-cyclopentyl n-C₄H₉ Ia.2874 H CH₂-cyclopentyl CH₂—CH═CH₂ Ia.2875 FCH₂-cyclopentyl CH₂—CH═CH₂ Ia.2876 Cl CH₂-cyclopentyl CH₂—CH═CH₂ Ia.2877H CH₂-cyclopentyl CH₂—C≡CH Ia.2878 F CH₂-cyclopentyl CH₂—C≡CH Ia.2879 ClCH₂-cyclopentyl CH₂—C≡CH Ia.2880 H CH₂-cyclopentyl CH₂—CO—OCH₃ Ia.2881 FCH₂-cyclopentyl CH₂—CO—OCH₃ Ia.2882 Cl CH₂-cyclopentyl CH₂—CO—OCH₃Ia.2883 H CH₂-cyclopentyl CH₂-phenyl Ia.2884 F CH₂-cyclopentylCH₂-phenyl Ia.2885 Cl CH₂-cyclopentyl CH₂-phenyl Ia.2886 HCH₂-cyclohexyl CH₃ Ia.2887 F CH₂-cyclohexyl CH₃ Ia.2888 ClCH₂-cyclohexyl CH₃ Ia.2889 H CH₂-cyclohexyl C₂H₅ Ia.2890 FCH₂-cyclohexyl C₂H₅ Ia.2891 Cl CH₂-cyclohexyl C₂H₅ Ia.2892 HCH₂-cyclohexyl n-C₃H₇ Ia.2893 F CH₂-cyclohexyl n-C₃H₇ Ia.2894 ClCH₂-cyclohexyl n-C₃H₇ Ia.2895 H CH₂-cyclohexyl n-C₄H₉ Ia.2896 FCH₂-cyclohexyl n-C₄H₉ Ia.2897 Cl CH₂-cyclohexyl n-C₄H₉ Ia.2898 HCH₂-cyclohexyl CH₂—CH═CH₂ Ia.2899 F CH₂-cyclohexyl CH₂—CH═CH₂ Ia.2900 ClCH₂-cyclohexyl CH₂—CH═CH₂ Ia.2901 H CH₂-cyclohexyl CH₂—C≡CH Ia.2902 FCH₂-cyclohexyl CH₂—C≡CH Ia.2903 Cl CH₂-cyclohexyl CH₂—C≡CH Ia.2904 HCH₂-cyclohexyl CH₂—CO—OCH₃ Ia.2905 F CH₂-cyclohexyl CH₂—CO—OCH₃ Ia.2906Cl CH₂-cyclohexyl CH₂—CO—OCH₃ Ia.2907 H CH₂-cyclohexyl CH₂-phenylIa.2908 F CH₂-cyclohexyl CH₂-phenyl Ia.2909 Cl CH₂-cyclohexyl CH₂-phenylIa.2910 H CH₂-phenyl CH₃ Ia.2911 F CH₂-phenyl CH₃ Ia.2912 Cl CH₂-phenylCH₃ Ia.2913 H CH₂-phenyl C₂H₅ Ia.2914 F CH₂-phenyl C₂H₅ Ia.2915 ClCH₂-phenyl C₂H₅ Ia.2916 H CH₂-phenyl n-C₃H₇ Ia.2917 F CH₂-phenyl n-C₃H₇Ia.2918 Cl CH₂-phenyl n-C₃H₇ Ia.2919 H CH₂-phenyl n-C₄H₉ Ia.2920 FCH₂-phenyl n-C₄H₉ Ia.2921 Cl CH₂-phenyl n-C₄H₉ Ia.2922 H CH₂-phenylCH₂—CH═CH₂ Ia.2923 F CH₂-phenyl CH₂—CH═CH₂ Ia.2924 Cl CH₂-phenylCH₂—CH═CH₂ Ia.2925 H CH₂-phenyl CH₂—C≡CH Ia.2926 F CH₂-phenyl CH₂—C≡CHIa.2927 Cl CH₂-phenyl CH₂—C≡CH Ia.2928 H CH₂-phenyl CH₂—CO—OCH₃ Ia.2929F CH₂-phenyl CH₂—CO—OCH₃ Ia.2930 Cl CH₂-phenyl CH₂—CO—OCH₃ Ia.2931 HCH₂-phenyl CH₂-phenyl Ia.2932 F CH₂-phenyl CH₂-phenyl Ia.2933 ClCH₂-phenyl CH₂-phenyl Ia.2934 H CH₂-(oxiran-2-yl) CH₃ Ia.2935 FCH₂-(oxiran-2-yl) CH₃ Ia.2936 Cl CH₂-(oxiran-2-yl) CH₃ Ia.2937 HCH₂-(oxiran-2-yl) C₂H₅ Ia.2938 F CH₂-(oxiran-2-yl) C₂H₅ Ia.2939 ClCH₂-(oxiran-2-yl) C₂H₅ Ia.2940 H CH₂-(oxiran-2-yl) n-C₃H₇ Ia.2941 FCH₂-(oxiran-2-yl) n-C₃H₇ Ia.2942 Cl CH₂-(oxiran-2-yl) n-C₃H₇ Ia.2943 HCH₂-(oxiran-2-yl) n-C₄H₉ Ia.2944 F CH₂-(oxiran-2-yl) n-C₄H₉ Ia.2945 ClCH₂-(oxiran-2-yl) n-C₄H₉ Ia.2946 H CH₂-(oxiran-2-yl) CH₂—CH═CH₂ Ia.2947F CH₂-(oxiran-2-yl) CH₂—CH═CH₂ Ia.2948 Cl CH₂-(oxiran-2-yl) CH₂—CH═CH₂Ia.2949 H CH₂-(oxiran-2-yl) CH₂—C≡CH Ia.2950 F CH₂-(oxiran-2-yl)CH₂—C≡CH Ia.2951 Cl CH₂-(oxiran-2-yl) CH₂—C≡CH Ia.2952 HCH₂-(oxiran-2-yl) CH₂—CO—OCH₃ Ia.2953 F CH₂-(oxiran-2-yl) CH₂—CO—OCH₃Ia.2954 Cl CH₂-(oxiran-2-yl) CH₂—CO—OCH₃ Ia.2955 H CH₂-(oxiran-2-yl)CH₂-phenyl Ia.2956 F CH₂-(oxiran-2-yl) CH₂-phenyl Ia.2957 ClCH₂-(oxiran-2-yl) CH₂-phenyl Ia.2958 H CH₂-(oxetan-3-yl) CH₃ Ia.2959 FCH₂-(oxetan-3-yl) CH₃ Ia.2960 Cl CH₂-(oxetan-3-yl) CH₃ Ia.2961 HCH₂-(oxetan-3-yl) C₂H₅ Ia.2962 F CH₂-(oxetan-3-yl) C₂H₅ Ia.2963 ClCH₂-(oxetan-3-yl) C₂H₅ Ia.2964 H CH₂-(oxetan-3-yl) n-C₃H₇ Ia.2965 FCH₂-(oxetan-3-yl) n-C₃H₇ Ia.2966 Cl CH₂-(oxetan-3-yl) n-C₃H₇ Ia.2967 HCH₂-(oxetan-3-yl) n-C₄H₉ Ia.2968 F CH₂-(oxetan-3-yl) n-C₄H₉ Ia.2969 ClCH₂-(oxetan-3-yl) n-C₄H₉ Ia.2970 H CH₂-(oxetan-3-yl) CH₂—CH═CH₂ Ia.2971F CH₂-(oxetan-3-yl) CH₂—CH═CH₂ Ia.2972 Cl CH₂-(oxetan-3-yl) CH₂—CH═CH₂Ia.2973 H CH₂-(oxetan-3-yl) CH₂—C≡CH Ia.2974 F CH₂-(oxetan-3-yl)CH₂—C≡CH Ia.2975 Cl CH₂-(oxetan-3-yl) CH₂—C≡CH Ia.2976 HCH₂-(oxetan-3-yl) CH₂—CO—OCH₃ Ia.2977 F CH₂-(oxetan-3-yl) CH₂—CO—OCH₃Ia.2978 Cl CH₂-(oxetan-3-yl) CH₂—CO—OCH₃ Ia.2979 H CH₂-(oxetan-3-yl)CH₂-phenyl Ia.2980 F CH₂-(oxetan-3-yl) CH₂-phenyl Ia.2981 ClCH₂-(oxetan-3-yl) CH₂-phenyl Ia.2982 H CH₂—CH₂-(pyrrolidin-1-yl) CH₃Ia.2983 F CH₂—CH₂-(pyrrolidin-1-yl) CH₃ Ia.2984 ClCH₂—CH₂-(pyrrolidin-1-yl) CH₃ Ia.2985 H CH₂—CH₂-(pyrrolidin-1-yl) C₂H₅Ia.2986 F CH₂—CH₂-(pyrrolidin-1-yl) C₂H₅ Ia.2987 ClCH₂—CH₂-(pyrrolidin-1-yl) C₂H₅ Ia.2988 H CH₂—CH₂-(pyrrolidin-1-yl)n-C₃H₇ Ia.2989 F CH₂—CH₂-(pyrrolidin-1-yl) n-C₃H₇ Ia.2990 ClCH₂—CH₂-(pyrrolidin-1-yl) n-C₃H₇ Ia.2991 H CH₂—CH₂-(pyrrolidin-1-yl)n-C₄H₉ Ia.2992 F CH₂—CH₂-(pyrrolidin-1-yl) n-C₄H₉ Ia.2993 ClCH₂—CH₂-(pyrrolidin-1-yl) n-C₄H₉ Ia.2994 H CH₂—CH₂-(pyrrolidin-1-yl)CH₂—CH═CH₂ Ia.2995 F CH₂—CH₂-(pyrrolidin-1-yl) CH₂—CH═CH₂ Ia.2996 ClCH₂—CH₂-(pyrrolidin-1-yl) CH₂—CH═CH₂ Ia.2997 H CH₂—CH₂-(pyrrolidin-1-yl)CH₂—C≡CH Ia.2998 F CH₂—CH₂-(pyrrolidin-1-yl) CH₂—C≡CH Ia.2999 ClCH₂—CH₂-(pyrrolidin-1-yl) CH₂—C≡CH Ia.3000 H CH₂—CH₂-(pyrrolidin-1-yl)CH₂—CO—OCH₃ Ia.3001 F CH₂—CH₂-(pyrrolidin-1-yl) CH₂—CO—OCH₃ Ia.3002 ClCH₂—CH₂-(pyrrolidin-1-yl) CH₂—CO—OCH₃ Ia.3003 HCH₂—CH₂-(pyrrolidin-1-yl) CH₂-phenyl Ia.3004 F CH₂—CH₂-(pyrrolidin-1-yl)CH₂-phenyl Ia.3005 Cl CH₂—CH₂-(pyrrolidin-1-yl) CH₂-phenyl Ia.3006 HCH₂-(pyridin-2-yl) CH₃ Ia.3007 F CH₂-(pyridin-2-yl) CH₃ Ia.3008 ClCH₂-(pyridin-2-yl) CH₃ Ia.3009 H CH₂-(pyridin-2-yl) C₂H₅ Ia.3010 FCH₂-(pyridin-2-yl) C₂H₅ Ia.3011 Cl CH₂-(pyridin-2-yl) C₂H₅ Ia.3012 HCH₂-(pyridin-2-yl) n-C₃H₇ Ia.3013 F CH₂-(pyridin-2-yl) n-C₃H₇ Ia.3014 ClCH₂-(pyridin-2-yl) n-C₃H₇ Ia.3015 H CH₂-(pyridin-2-yl) n-C₄H₉ Ia.3016 FCH₂-(pyridin-2-yl) n-C₄H₉ Ia.3017 Cl CH₂-(pyridin-2-yl) n-C₄H₉ Ia.3018 HCH₂-(pyridin-2-yl) CH₂—CH═CH₂ Ia.3019 F CH₂-(pyridin-2-yl) CH₂—CH═CH₂Ia.3020 Cl CH₂-(pyridin-2-yl) CH₂—CH═CH₂ Ia.3021 H CH₂-(pyridin-2-yl)CH₂—C≡CH Ia.3022 F CH₂-(pyridin-2-yl) CH₂—C≡CH Ia.3023 ClCH₂-(pyridin-2-yl) CH₂—C≡CH Ia.3024 H CH₂-(pyridin-2-yl) CH₂—CO—OCH₃Ia.3025 F CH₂-(pyridin-2-yl) CH₂—CO—OCH₃ Ia.3026 Cl CH₂-(pyridin-2-yl)CH₂—CO—OCH₃ Ia.3027 H CH₂-(pyridin-2-yl) CH₂-phenyl Ia.3028 FCH₂-(pyridin-2-yl) CH₂-phenyl Ia.3029 Cl CH₂-(pyridin-2-yl) CH₂-phenylIa.3030 H CH₃ CH₂—CH₂—Cl Ia.3031 F CH₃ CH₂—CH₂—Cl Ia.3032 Cl CH₃CH₂—CH₂—Cl Ia.3033 H C₂H₅ CH₂—CH₂—Cl Ia.3034 F C₂H₅ CH₂—CH₂—Cl Ia.3035Cl C₂H₅ CH₂—CH₂—Cl Ia.3036 H n-C₃H₇ CH₂—CH₂—Cl Ia.3037 F n-C₃H₇CH₂—CH₂—Cl Ia.3038 Cl n-C₃H₇ CH₂—CH₂—Cl Ia.3039 H n-C₄H₉ CH₂—CH₂—ClIa.3040 F n-C₄H₉ CH₂—CH₂—Cl Ia.3041 Cl n-C₄H₉ CH₂—CH₂—Cl Ia.3042 HCH₂—CH═CH₂ CH₂—CH₂—Cl Ia.3043 F CH₂—CH═CH₂ CH₂—CH₂—Cl Ia.3044 ClCH₂—CH═CH₂ CH₂—CH₂—Cl Ia.3045 H CH₂—C≡CH CH₂—CH₂—Cl Ia.3046 F CH₂—C≡CHCH₂—CH₂—Cl Ia.3047 Cl CH₂—C≡CH CH₂—CH₂—Cl Ia.3048 H CH₂—CO—OCH₃CH₂—CH₂—Cl Ia.3049 F CH₂—CO—OCH₃ CH₂—CH₂—Cl Ia.3050 Cl CH₂—CO—OCH₃CH₂—CH₂—Cl Ia.3051 H CH₂-phenyl CH₂—CH₂—Cl Ia.3052 F CH₂-phenylCH₂—CH₂—Cl Ia.3053 Cl CH₂-phenyl CH₂—CH₂—Cl Ia.3054 H CH₃ CH₂—CF₃Ia.3055 F CH₃ CH₂—CF₃ Ia 3056 Cl CH₃ CH₂—CF₃ Ia.3057 H C₂H₅ CH₂—CF₃Ia.3058 F C₂H₅ CH₂—CF₃ Ia.3059 Cl C₂H₅ CH₂—CF₃ Ia.3060 H n-C₃H₇ CH₂—CF₃Ia.3061 F n-C₃H₇ CH₂—CF₃ Ia.3062 Cl n-C₃H₇ CH₂—CF₃ Ia.3063 H n-C₄H₉CH₂—CF₃ Ia.3064 F n-C₄H₉ CH₂—CF₃ Ia.3065 Cl n-C₄H₉ CH₂—CF₃ Ia.3066 HCH₂—CH═CH₂ CH₂—CF₃ Ia.3067 F CH₂—CH═CH₂ CH₂—CF₃ Ia.3068 Cl CH₂—CH═CH₂CH₂—CF₃ Ia.3069 H CH₂—C≡CH CH₂—CF₃ Ia.3070 F CH₂—C≡CH CH₂—CF₃ Ia.3071 ClCH₂—C≡CH CH₂—CF₃ Ia.3072 H CH₂—CO—OCH₃ CH₂—CF₃ Ia.3073 F CH₂—CO—OCH₃CH₂—CF₃ Ia.3074 Cl CH₂—CO—OCH₃ CH₂—CF₃ Ia.3075 H CH₂-phenyl CH₂—CF₃Ia.3076 F CH₂-phenyl CH₂—CF₃ Ia.3077 Cl CH₂-phenyl CH₂—CF₃ Ia.3078 H CH₃CH₂—CH₂—OH Ia.3079 F CH₃ CH₂—CH₂—OH Ia.3080 Cl CH₃ CH₂—CH₂—OH Ia.3081 HC₂H₅ CH₂—CH₂—OH Ia.3082 F C₂H₅ CH₂—CH₂—OH Ia.3083 Cl C₂H₅ CH₂—CH₂—OHIa.3084 H n-C₃H₇ CH₂—CH₂—OH Ia.3085 F n-C₃H₇ CH₂—CH₂—OH Ia.3086 Cln-C₃H₇ CH₂—CH₂—OH Ia.3087 H n-C₄H₉ CH₂—CH₂—OH Ia.3088 F n-C₄H₉CH₂—CH₂—OH Ia.3089 Cl n-C₄H₉ CH₂—CH₂—OH Ia.3090 H CH₂—CH═CH₂ CH₂—CH₂—OHIa.3091 F CH₂—CH═CH₂ CH₂—CH₂—OH Ia.3092 Cl CH₂—CH═CH₂ CH₂—CH₂—OH Ia.3093H CH₂—C≡CH CH₂—CH₂—OH Ia.3094 F CH₂—C≡CH CH₂—CH₂—OH Ia.3095 Cl CH₂—C≡CHCH₂—CH₂—OH Ia.3096 H CH₂—CO—OCH₃ CH₂—CH₂—OH Ia.3097 F CH₂—CO—OCH₃CH₂—CH₂—OH Ia.3098 Cl CH₂—CO—OCH₃ CH₂—CH₂—OH Ia.3099 H CH₂-phenylCH₂—CH₂—OH Ia.3100 F CH₂-phenyl CH₂—CH₂—OH Ia.3101 Cl CH₂-phenylCH₂—CH₂—OH Ia.3102 H CH₃ CH₂—CH(CH₃)—OH Ia.3103 F CH₃ CH₂—CH(CH₃)—OHIa.3104 Cl CH₃ CH₂—CH(CH₃)—OH Ia.3105 H C₂H₅ CH₂—CH(CH₃)—OH Ia.3106 FC₂H₅ CH₂—CH(CH₃)—OH Ia.3107 Cl C₂H₅ CH₂—CH(CH₃)—OH Ia.3108 H n-C₃H₇CH₂—CH(CH₃)—OH Ia.3109 F n-C₃H₇ CH₂—CH(CH₃)—OH Ia.3110 Cl n-C₃H₇CH₂—CH(CH₃)—OH Ia.3111 H n-C₄H₉ CH₂—CH(CH₃)—OH Ia.3112 F n-C₄H₉CH₂—CH(CH₃)—OH Ia.3113 Cl n-C₄H₉ CH₂—CH(CH₃)—OH Ia.3114 H CH₂—CH═CH₂CH₂—CH(CH₃)—OH Ia.3115 F CH₂—CH═CH₂ CH₂—CH(CH₃)—OH Ia.3116 Cl CH₂—CH═CH₂CH₂—CH(CH₃)—OH Ia.3117 H CH₂—C≡CH CH₂—CH(CH₃)—OH Ia.3118 F CH₂—C≡CHCH₂—CH(CH₃)—OH Ia.3119 Cl CH₂—C≡CH CH₂—CH(CH₃)—OH Ia.3120 H CH₂—CO—OCH₃CH₂—CH(CH₃)—OH Ia.3121 F CH₂—CO—OCH₃ CH₂—CH(CH₃)—OH Ia.3122 ClCH₂—CO—OCH₃ CH₂—CH(CH₃)—OH Ia.3123 H CH₂-phenyl CH₂—CH(CH₃)—OH Ia.3124 FCH₂-phenyl CH₂—CH(CH₃)—OH Ia.3125 Cl CH₂-phenyl CH₂—CH(CH₃)—OH Ia.3126 HCH₃ CH₂—CH₂—CN Ia.3127 F CH₃ CH₂—CH₂—CN Ia.3128 Cl CH₃ CH₂—CH₂—CNIa.3129 H C₂H₅ CH₂—CH₂—CN Ia.3130 F C₂H₅ CH₂—CH₂—CN Ia.3131 Cl C₂H₅CH₂—CH₂—CN Ia.3132 H n-C₃H₇ CH₂—CH₂—CN Ia.3133 F n-C₃H₇ CH₂—CH₂—CNIa.3134 Cl n-C₃H₇ CH₂—CH₂—CN Ia.3135 H n-C₄H₉ CH₂—CH₂—CN Ia.3136 Fn-C₄H₉ CH₂—CH₂—CN Ia.3137 Cl n-C₄H₉ CH₂—CH₂—CN Ia.3138 H CH₂—CH═CH₂CH₂—CH₂—CN Ia.3139 F CH₂—CH═CH₂ CH₂—CH₂—CN Ia.3140 Cl CH₂—CH═CH₂CH₂—CH₂—CN Ia.3141 H CH₂—C≡CH CH₂—CH₂—CN Ia.3142 F CH₂—C≡CH CH₂—CH₂—CNIa.3143 Cl CH₂—C≡CH CH₂—CH₂—CN Ia.3144 H CH₂—CO—OCH₃ CH₂—CH₂—CN Ia.3145F CH₂—CO—OCH₃ CH₂—CH₂—CN Ia.3146 Cl CH₂—CO—OCH₃ CH₂—CH₂—CN Ia.3147 HCH₂-phenyl CH₂—CH₂—CN Ia.3148 F CH₂-phenyl CH₂—CH₂—CN Ia.3149 ClCH₂-phenyl CH₂—CH₂—CN Ia.3150 H CH₃ CH₂—OCH₃ Ia.3151 F CH₃ CH₂—OCH₃Ia.3152 Cl CH₃ CH₂—OCH₃ Ia.3153 H C₂H₅ CH₂—OCH₃ Ia.3154 F C₂H₅ CH₂—OCH₃Ia.3155 Cl C₂H₅ CH₂—OCH₃ Ia.3156 H n-C₃H₇ CH₂—OCH₃ Ia.3157 F n-C₃H₇CH₂—OCH₃ Ia.3158 Cl n-C₃H₇ CH₂—OCH₃ Ia.4219 H n-C₄H₉ CH₂—OCH₃ Ia.4220 Fn-C₄H₉ CH₂—OCH₃ Ia.4221 Cl n-C₄H₉ CH₂—OCH₃ Ia.4222 H CH₂—CH═CH₂ CH₂—OCH₃Ia.4223 F CH₂—CH═CH₂ CH₂—OCH₃ Ia.4224 Cl CH₂—CH═CH₂ CH₂—OCH₃ Ia.4225 HCH₂—C≡CH CH₂—OCH₃ Ia.4226 F CH₂—C≡CH CH₂—OCH₃ Ia.4227 Cl CH₂—C≡CHCH₂—OCH₃ Ia.4228 H CH₂—CO—OCH₃ CH₂—OCH₃ Ia.4229 F CH₂—CO—OCH₃ CH₂—OCH₃Ia.4230 Cl CH₂—CO—OCH₃ CH₂—OCH₃ Ia.4231 H CH₂-phenyl CH₂—OCH₃ Ia.4232 FCH₂-phenyl CH₂—OCH₃ Ia.4233 Cl CH₂-phenyl CH₂—OCH₃ Ia.4234 H CH₃CH₂—CH₂—OCH₃ Ia.4235 F CH₃ CH₂—CH₂—OCH₃ Ia.4236 Cl CH₃ CH₂—CH₂—OCH₃Ia.4237 H C₂H₅ CH₂—CH₂—OCH₃ Ia.4238 F C₂H₅ CH₂—CH₂—OCH₃ Ia.4239 Cl C₂H₅CH₂—CH₂—OCH₃ Ia.4240 H n-C₃H₇ CH₂—CH₂—OCH₃ Ia.4241 F n-C₃H₇ CH₂—CH₂—OCH₃Ia.4242 Cl n-C₃H₇ CH₂—CH₂—OCH₃ Ia.4243 H n-C₄H₉ CH₂—CH₂—OCH₃ Ia.4244 Fn-C₄H₉ CH₂—CH₂—OCH₃ Ia.4245 Cl n-C₄H₉ CH₂—CH₂—OCH₃ Ia.4246 H CH₂—CH═CH₂CH₂—CH₂—OCH₃ Ia.4247 F CH₂—CH═CH₂ CH₂—CH₂—OCH₃ Ia.4248 Cl CH₂—CH═CH₂CH₂—CH₂—OCH₃ Ia.4249 H CH₂—C≡CH CH₂—CH₂—OCH₃ Ia.4250 F CH₂—C≡CHCH₂—CH₂—OCH₃ Ia.4251 Cl CH₂—C≡CH CH₂—CH₂—OCH₃ Ia.4252 H CH₂—CO—OCH₃CH₂—CH₂—OCH₃ Ia.4253 F CH₂—CO—OCH₃ CH₂—CH₂—OCH₃ Ia.4254 Cl CH₂—CO—OCH₃CH₂—CH₂—OCH₃ Ia.4255 H CH₂-phenyl CH₂—CH₂—OCH₃ Ia.4256 F CH₂-phenylCH₂—CH₂—OCH₃ Ia.4257 Cl CH₂-phenyl CH₂—CH₂—OCH₃ Ia.4258 H CH₃CH₂—CH₂—OCH₂—CH═CH₂ Ia.4259 F CH₃ CH₂—CH₂—OCH₂—CH═CH₂ Ia.4260 Cl CH₃CH₂—CH₂—OCH₂—CH═CH₂ Ia.4261 H C₂H₅ CH₂—CH₂—OCH₂—CH═CH₂ Ia.4262 F C₂H₅CH₂—CH₂—OCH₂—CH═CH₂ Ia.4263 Cl C₂H₅ CH₂—CH₂—OCH₂—CH═CH₂ Ia.4264 H n-C₃H₇CH₂—CH₂—OCH₂—CH═CH₂ Ia.4265 F n-C₃H₇ CH₂—CH₂—OCH₂—CH═CH₂ Ia.4266 Cln-C₃H₇ CH₂—CH₂—OCH₂—CH═CH₂ Ia.4267 H n-C₄H₉ CH₂—CH₂—OCH₂—CH═CH₂ Ia.4268F n-C₄H₉ CH₂—CH₂—OCH₂—CH═CH₂ Ia.4269 Cl n-C₄H₉ CH₂—CH₂—OCH₂—CH═CH₂Ia.4270 H CH₂—CH═CH₂ CH₂—CH₂—OCH₂—CH═CH₂ Ia.4271 F CH₂—CH═CH₂CH₂—CH₂—OCH₂—CH═CH₂ Ia.4272 Cl CH₂—CH═CH₂ CH₂—CH₂—OCH₂—CH═CH₂ Ia.4273 HCH₂—C≡CH CH₂—CH₂—OCH₂—CH═CH₂ Ia.4274 F CH₂—C≡CH CH₂—CH₂—OCH₂—CH═CH₂Ia.4275 Cl CH₂—C≡CH CH₂—CH₂—OCH₂—CH═CH₂ Ia.4276 H CH₂—CO—OCH₃CH₂—CH₂—OCH₂—CH═CH₂ Ia.4277 F CH₂—CO—OCH₃ CH₂—CH₂—OCH₂—CH═CH₂ Ia.4278 ClCH₂—CO—OCH₃ CH₂—CH₂—OCH₂—CH═CH₂ Ia.4279 H CH₂-phenyl CH₂—CH₂—OCH₂—CH═CH₂Ia.4280 F CH₂-phenyl CH₂—CH₂—OCH₂—CH═CH₂ Ia.4281 Cl CH₂-phenylCH₂—CH₂—OCH₂—CH═CH₂ Ia.4282 H CH₃ CH₂—CH₂—O-cyclopentyl Ia.4283 F CH₃CH₂—CH₂—O-cyclopentyl Ia.4284 Cl CH₃ CH₂—CH₂—O-cyclopentyl Ia.4285 HC₂H₅ CH₂—CH₂—O-cyclopentyl Ia.4286 F C₂H₅ CH₂—CH₂—O-cyclopentyl Ia.4287Cl C₂H₅ CH₂—CH₂—O-cyclopentyl Ia.4288 H n-C₃H₇ CH₂—CH₂—O-cyclopentylIa.4289 F n-C₃H₇ CH₂—CH₂—O-cyclopentyl Ia.4290 Cl n-C₃H₇CH₂—CH₂—O-cyclopentyl Ia.4291 H n-C₄H₉ CH₂—CH₂—O-cyclopentyl Ia.4292 Fn-C₄H₉ CH₂—CH₂—O-cyclopentyl Ia.4293 Cl n-C₄H₉ CH₂—CH₂—O-cyclopentylIa.4294 H CH₂—CH═CH₂ CH₂—CH₂—O-cyclopentyl Ia.4295 F CH₂—CH═CH₂CH₂—CH₂—O-cyclopentyl Ia.4296 Cl CH₂—CH═CH₂ CH₂—CH₂—O-cyclopentylIa.4297 H CH₂—C≡CH CH₂—CH₂—O-cyclopentyl Ia.4298 F CH₂—C≡CHCH₂—CH₂—O-cyclopentyl Ia.4299 Cl CH₂—C≡CH CH₂—CH₂—O-cyclopentyl Ia.4300H CH₂—CO—OCH₃ CH₂—CH₂—O-cyclopentyl Ia.4301 F CH₂—CO—OCH₃CH₂—CH₂—O-cyclopentyl Ia.4302 Cl CH₂—CO—OCH₃ CH₂—CH₂—O-cyclopentylIa.4303 H CH₂-phenyl CH₂—CH₂—O-cyclopentyl Ia.4304 F CH₂-phenylCH₂—CH₂—O-cyclopentyl Ia.4305 Cl CH₂-phenyl CH₂—CH₂—O-cyclopentylIa.4306 H CH₃ CH₂—CH₂—N(CH₃)₂ Ia.4307 F CH₃ CH₂—CH₂—N(CH₃)₂ Ia.4308 ClCH₃ CH₂—CH₂—N(CH₃)₂ Ia.4309 H C₂H₅ CH₂—CH₂—N(CH₃)₂ Ia.4310 F C₂H₅CH₂—CH₂—N(CH₃)₂ Ia.4311 Cl C₂H₅ CH₂—CH₂—N(CH₃)₂ Ia.4312 H n-C₃H₇CH₂—CH₂—N(CH₃)₂ Ia.4313 F n-C₃H₇ CH₂—CH₂—N(CH₃)₂ Ia.4314 Cl n-C₃H₇CH₂—CH₂—N(CH₃)₂ Ia.4315 H n-C₄H₉ CH₂—CH₂—N(CH₃)₂ Ia.4316 F n-C₄H₉CH₂—CH₂—N(CH₃)₂ Ia.4317 Cl n-C₄H₉ CH₂—CH₂—N(CH₃)₂ Ia.4318 H CH₂—CH═CH₂CH₂—CH₂—N(CH₃)₂ Ia.4319 F CH₂—CH═CH₂ CH₂—CH₂—N(CH₃)₂ Ia.4320 ClCH₂—CH═CH₂ CH₂—CH₂—N(CH₃)₂ Ia.4321 H CH₂—C≡CH CH₂—CH₂—N(CH₃)₂ Ia.4322 FCH₂—C≡CH CH₂—CH₂—N(CH₃)₂ Ia.4323 Cl CH₂—C≡CH CH₂—CH₂—N(CH₃)₂ Ia.4324 HCH₂—CO—OCH₃ CH₂—CH₂—N(CH₃)₂ Ia.4325 F CH₂—CO—OCH₃ CH₂—CH₂—N(CH₃)₂Ia.4326 Cl CH₂—CO—OCH₃ CH₂—CH₂—N(CH₃)₂ Ia.4327 H CH₂-phenylCH₂—CH₂—N(CH₃)₂ Ia.4328 F CH₂-phenyl CH₂—CH₂—N(CH₃)₂ Ia.4329 ClCH₂-phenyl CH₂—CH₂—N(CH₃)₂ Ia.4330 H CH₃ CH₂—CH₂—SCH₃ Ia.4331 F CH₃CH₂—CH₂—SCH₃ Ia.4332 Cl CH₃ CH₂—CH₂—SCH₃ Ia.4333 H C₂H₅ CH₂—CH₂—SCH₃Ia.4334 F C₂H₅ CH₂—CH₂—SCH₃ Ia.4335 Cl C₂H₅ CH₂—CH₂—SCH₃ Ia.4336 Hn-C₃H₇ CH₂—CH₂—SCH₃ Ia.4337 F n-C₃H₇ CH₂—CH₂—SCH₃ Ia.4338 Cl n-C₃H₇CH₂—CH₂—SCH₃ Ia.4339 H n-C₄H₉ CH₂—CH₂—SCH₃ Ia.4340 F n-C₄H₉ CH₂—CH₂—SCH₃Ia.4341 Cl n-C₄H₉ CH₂—CH₂—SCH₃ Ia.4342 H CH₂—CH═CH₂ CH₂—CH₂—SCH₃ Ia.4343F CH₂—CH═CH₂ CH₂—CH₂—SCH₃ Ia.4344 Cl CH₂—CH═CH₂ CH₂—CH₂—SCH₃ Ia.4345 HCH₂—C≡CH CH₂—CH₂—SCH₃ Ia.4346 F CH₂—C≡CH CH₂—CH₂—SCH₃ Ia.4347 ClCH₂—C≡CH CH₂—CH₂—SCH₃ Ia.4348 H CH₂—CO—OCH₃ CH₂—CH₂—SCH₃ Ia.4349 FCH₂—CO—OCH₃ CH₂—CH₂—SCH₃ Ia.4350 Cl CH₂—CO—OCH₃ CH₂—CH₂—SCH₃ Ia.4351 HCH₂-phenyl CH₂—CH₂—SCH₃ Ia.4352 F CH₂-phenyl CH₂—CH₂—SCH₃ Ia.4353 ClCH₂-phenyl CH₂—CH₂—SCH₃ Ia.4354 H CH₃ CH₂—CH₂—SO₂—CH₃ Ia.4355 F CH₃CH₂—CH₂—SO₂—CH₃ Ia.4356 Cl CH₃ CH₂—CH₂—SO₂—CH₃ Ia.4357 H C₂H₅CH₂—CH₂—SO₂—CH₃ Ia.4358 F C₂H₅ CH₂—CH₂—SO₂—CH₃ Ia.4359 Cl C₂H₅CH₂—CH₂—SO₂—CH₃ Ia.4360 H n-C₃H₇ CH₂—CH₂—SO₂—CH₃ Ia.4361 F n-C₃H₇CH₂—CH₂—SO₂—CH₃ Ia.4362 Cl n-C₃H₇ CH₂—CH₂—SO₂—CH₃ Ia.4363 H n-C₄H₉CH₂—CH₂—SO₂—CH₃ Ia.4364 F n-C₄H₉ CH₂—CH₂—SO₂—CH₃ Ia.4365 Cl n-C₄H₉CH₂—CH₂—SO₂—CH₃ Ia.4366 H CH₂—CH═CH₂ CH₂—CH₂—SO₂—CH₃ Ia.4367 FCH₂—CH═CH₂ CH₂—CH₂—SO₂—CH₃ Ia.4368 Cl CH₂—CH═CH₂ CH₂—CH₂—SO₂—CH₃ Ia.4369H CH₂—C≡CH CH₂—CH₂—SO₂—CH₃ Ia.4370 F CH₂—C≡CH CH₂—CH₂—SO₂—CH₃ Ia.4371 ClCH₂—C≡CH CH₂—CH₂—SO₂—CH₃ Ia.4372 H CH₂—CO—OCH₃ CH₂—CH₂—SO₂—CH₃ Ia.4373 FCH₂—CO—OCH₃ CH₂—CH₂—SO₂—CH₃ Ia.4374 Cl CH₂—CO—OCH₃ CH₂—CH₂—SO₂—CH₃Ia.4375 H CH₂-phenyl CH₂—CH₂—SO₂—CH₃ Ia.4376 F CH₂-phenylCH₂—CH₂—SO₂—CH₃ Ia.4377 Cl CH₂-phenyl CH₂—CH₂—SO₂—CH₃ Ia.4378 H CH₃CH₂—CH═CH₂ Ia.4379 F CH₃ CH₂—CH═CH₂ Ia.4380 Cl CH₃ CH₂—CH═CH₂ Ia.4381 HC₂H₅ CH₂—CH═CH₂ Ia.4382 F C₂H₅ CH₂—CH═CH₂ Ia.4383 Cl C₂H₅ CH₂—CH═CH₂Ia.4384 H n-C₃H₇ CH₂—CH═CH₂ Ia.4385 F n-C₃H₇ CH₂—CH═CH₂ Ia.4386 Cln-C₃H₇ CH₂—CH═CH₂ Ia.4387 H n-C₄H₉ CH₂—CH═CH₂ Ia.4388 F n-C₄H₉CH₂—CH═CH₂ Ia.4389 Cl n-C₄H₉ CH₂—CH═CH₂ Ia.4390 H CH₃ CH₂—CH═CH—CH₃Ia.4391 F CH₃ CH₂—CH═CH—CH₃ Ia.4392 Cl CH₃ CH₂—CH═CH—CH₃ Ia.4393 H C₂H₅CH₂—CH═CH—CH₃ Ia.4394 F C₂H₅ CH₂—CH═CH—CH₃ Ia.4395 Cl C₂H₅ CH₂—CH═CH—CH₃Ia.4396 H n-C₃H₇ CH₂—CH═CH—CH₃ Ia.4397 F n-C₃H₇ CH₂—CH═CH—CH₃ Ia.4398 Cln-C₃H₇ CH₂—CH═CH—CH₃ Ia.4399 H n-C₄H₉ CH₂—CH═CH—CH₃ Ia.4400 F n-C₄H₉CH₂—CH═CH—CH₃ Ia.4401 Cl n-C₄H₉ CH₂—CH═CH—CH₃ Ia.4402 H CH₂—CH═CH₂CH₂—CH═CH—CH₃ Ia.4403 F CH₂—CH═CH₂ CH₂—CH═CH—CH₃ Ia.4404 Cl CH₂—CH═CH₂CH₂—CH═CH—CH₃ Ia.4405 H CH₂—C≡CH CH₂—CH═CH—CH₃ Ia.4406 F CH₂—C≡CHCH₂—CH═CH—CH₃ Ia.4407 Cl CH₂—C≡CH CH₂—CH═CH—CH₃ Ia.4408 H CH₂—CO—OCH₃CH₂—CH═CH—CH₃ Ia.4409 F CH₂—CO—OCH₃ CH₂—CH═CH—CH₃ Ia.4410 Cl CH₂—CO—OCH₃CH₂—CH═CH—CH₃ Ia.4411 H CH₂-phenyl CH₂—CH═CH—CH₃ Ia.4412 F CH₂-phenylCH₂—CH═CH—CH₃ Ia.4413 Cl CH₂-phenyl CH₂—CH═CH—CH₃ Ia.4414 H CH₃CH₂—CH═CH—Cl Ia.4415 F CH₃ CH₂—CH═CH—Cl Ia.4416 Cl CH₃ CH₂—CH═CH—ClIa.4417 H C₂H₅ CH₂—CH═CH—Cl Ia.4418 F C₂H₅ CH₂—CH═CH—Cl Ia.4419 Cl C₂H₅CH₂—CH═CH—Cl Ia.4420 H n-C₃H₇ CH₂—CH═CH—Cl Ia.4421 F n-C₃H₇ CH₂—CH═CH—ClIa.4422 Cl n-C₃H₇ CH₂—CH═CH—Cl Ia.4423 H n-C₄H₉ CH₂—CH═CH—Cl Ia.4424 Fn-C₄H₉ CH₂—CH═CH—Cl Ia.4425 Cl n-C₄H₉ CH₂—CH═CH—Cl Ia.4426 H CH₂—CH═CH₂CH₂—CH═CH—Cl Ia.4427 F CH₂—CH═CH₂ CH₂—CH═CH—Cl Ia.4428 Cl CH₂—CH═CH₂CH₂—CH═CH—Cl Ia.4429 H CH₂—C≡CH CH₂—CH═CH—Cl Ia.4430 F CH₂—C≡CHCH₂—CH═CH—Cl Ia.4431 Cl CH₂—C≡CH CH₂—CH═CH—Cl Ia.4432 H CH₂—CO—OCH₃CH₂—CH═CH—Cl Ia.4433 F CH₂—CO—OCH₃ CH₂—CH═CH—Cl Ia.4434 Cl CH₂—CO—OCH₃CH₂—CH═CH—Cl Ia.4435 H CH₂-phenyl CH₂—CH═CH—Cl Ia.4436 F CH₂-phenylCH₂—CH═CH—Cl Ia.4437 Cl CH₂-phenyl CH₂—CH═CH—Cl Ia.4438 H CH₃ CH₂—C≡CHIa.4439 F CH₃ CH₂—C≡CH Ia.4440 Cl CH₃ CH₂—C≡CH Ia.4441 H C₂H₅ CH₂—C≡CHIa.4442 F C₂H₅ CH₂—C≡CH Ia.4443 Cl C₂H₅ CH₂—C≡CH Ia.4444 H n-C₃H₇CH₂—C≡CH Ia.4445 F n-C₃H₇ CH₂—C≡CH Ia.4446 Cl n-C₃H₇ CH₂—C≡CH Ia.4447 Hn-C₄H₉ CH₂—C≡CH Ia.4448 F n-C₄H₉ CH₂—C≡CH Ia.4449 Cl n-C₄H₉ CH₂—C≡CHIa.4450 H CH₃ CH₂—CH═N—OCH₃ Ia.4451 F CH₃ CH₂—CH═N—OCH₃ Ia.4452 Cl CH₃CH₂—CH═N—OCH₃ Ia.4453 H C₂H₅ CH₂—CH═N—OCH₃ Ia.4454 F C₂H₅ CH₂—CH═N—OCH₃Ia.4455 Cl C₂H₅ CH₂—CH═N—OCH₃ Ia.4456 H n-C₃H₇ CH₂—CH═N—OCH₃ Ia.4457 Fn-C₃H₇ CH₂—CH═N—OCH₃ Ia.4458 Cl n-C₃H₇ CH₂—CH═N—OCH₃ Ia.4459 H n-C₄H₉CH₂—CH═N—OCH₃ Ia.4460 F n-C₄H₉ CH₂—CH═N—OCH₃ Ia.4461 Cl n-C₄H₉CH₂—CH═N—OCH₃ Ia.4462 H CH₂—CH═CH₂ CH₂—CH═N—OCH₃ Ia.4463 F CH₂—CH═CH₂CH₂—CH═N—OCH₃ Ia.4464 Cl CH₂—CH═CH₂ CH₂—CH═N—OCH₃ Ia.4465 H CH₂—C≡CHCH₂—CH═N—OCH₃ Ia.4466 F CH₂—C≡CH CH₂—CH═N—OCH₃ Ia.4467 Cl CH₂—C≡CHCH₂—CH═N—OCH₃ Ia.4468 H CH₂—CO—OCH₃ CH₂—CH═N—OCH₃ Ia.4469 F CH₂—CO—OCH₃CH₂—CH═N—OCH₃ Ia.4470 Cl CH₂—CO—OCH₃ CH₂—CH═N—OCH₃ Ia.4471 H CH₂-phenylCH₂—CH═N—OCH₃ Ia.4472 F CH₂-phenyl CH₂—CH═N—OCH₃ Ia.4473 Cl CH₂-phenylCH₂—CH═N—OCH₃ Ia.4474 H CH₃ CH₂—CH═N—OC₂H₅ Ia.4475 F CH₃ CH₂—CH═N—OC₂H₅Ia.4476 Cl CH₃ CH₂—CH═N—OC₂H₅ Ia.4477 H C₂H₅ CH₂—CH═N—OC₂H₅ Ia.4478 FC₂H₅ CH₂—CH═N—OC₂H₅ Ia.4479 Cl C₂H₅ CH₂—CH═N—OC₂H₅ Ia.4480 H n-C₃H₇CH₂—CH═N—OC₂H₅ Ia.4481 F n-C₃H₇ CH₂—CH═N—OC₂H₅ Ia.4482 Cl n-C₃H₇CH₂—CH═N—OC₂H₅ Ia.4483 H n-C₄H₉ CH₂—CH═N—OC₂H₅ Ia.4484 F n-C₄H₉CH₂—CH═N—OC₂H₅ Ia.4485 Cl n-C₄H₉ CH₂—CH═N—OC₂H₅ Ia.4486 H CH₂—CH═CH₂CH₂—CH═N—OC₂H₅ Ia.4487 F CH₂—CH═CH₂ CH₂—CH═N—OC₂H₅ Ia.4488 Cl CH₂—CH═CH₂CH₂—CH═N—OC₂H₅ Ia.4489 H CH₂—C≡CH CH₂—CH═N—OC₂H₅ Ia.4490 F CH₂—C≡CHCH₂—CH═N—OC₂H₅ Ia.4491 Cl CH₂—C≡CH CH₂—CH═N—OC₂H₅ Ia.4492 H CH₂—CO—OCH₃CH₂—CH═N—OC₂H₅ Ia.4493 F CH₂—CO—OCH₃ CH₂—CH═N—OC₂H₅ Ia.4494 ClCH₂—CO—OCH₃ CH₂—CH═N—OC₂H₅ Ia.4495 H CH₂-phenyl CH₂—CH═N—OC₂H₅ Ia.4496 FCH₂-phenyl CH₂—CH═N—OC₂H₅ Ia.4497 Cl CH₂-phenyl CH₂—CH═N—OC₂H₅ Ia.4498 HCH₃ CH₂—CH═N—O(n-C₃H₇) Ia.4499 F CH₃ CH₂—CH═N—O(n-C₃H₇) Ia.4500 Cl CH₃CH₂—CH═N—O(n-C₃H₇) Ia.4501 H C₂H₅ CH₂—CH═N—O(n-C₃H₇) Ia.4502 F C₂H₅CH₂—CH═N—O(n-C₃H₇) Ia.4503 Cl C₂H₅ CH₂—CH═N—O(n-C₃H₇) Ia.4504 H n-C₃H₇CH₂—CH═N—O(n-C₃H₇) Ia.4505 F n-C₃H₇ CH₂—CH═N—O(n-C₃H₇) Ia.4506 Cl n-C₃H₇CH₂—CH═N—O(n-C₃H₇) Ia.4507 H n-C₄H₉ CH₂—CH═N—O(n-C₃H₇) Ia.4508 F n-C₄H₉CH₂—CH═N—O(n-C₃H₇) Ia.4509 Cl n-C₄H₉ CH₂—CH═N—O(n-C₃H₇) Ia.4510 HCH₂—CH═CH₂ CH₂—CH═N—O(n-C₃H₇) Ia.4511 F CH₂—CH═CH₂ CH₂—CH═N—O(n-C₃H₇)Ia.4512 Cl CH₂—CH═CH₂ CH₂—CH═N—O(n-C₃H₇) Ia.4513 H CH₂—C≡CHCH₂—CH═N—O(n-C₃H₇) Ia.4514 F CH₂—C≡CH CH₂—CH═N—O(n-C₃H₇) Ia.4515 ClCH₂—C≡CH CH₂—CH═N—O(n-C₃H₇) Ia.4516 H CH₂—CO—OCH₃ CH₂—CH═N—O(n-C₃H₇)Ia.4517 F CH₂—CO—OCH₃ CH₂—CH═N—O(n-C₃H₇) Ia.4518 Cl CH₂—CO—OCH₃CH₂—CH═N—O(n-C₃H₇) Ia.4519 H CH₂-phenyl CH₂—CH═N—O(n-C₃H₇) Ia.4520 FCH₂-phenyl CH₂—CH═N—O(n-C₃H₇) Ia.4521 Cl CH₂-phenyl CH₂—CH═N—O(n-C₃H₇)Ia.4522 H CH₃ CH₂—CH═N—O(n-C₄H₉) Ia.4523 F CH₃ CH₂—CH═N—O(n-C₄H₉)Ia.4524 Cl CH₃ CH₂—CH═N—O(n-C₄H₉) Ia.4525 H C₂H₅ CH₂—CH═N—O(n-C₄H₉)Ia.4526 F C₂H₅ CH₂—CH═N—O(n-C₄H₉) Ia.4527 Cl C₂H₅ CH₂—CH═N—O(n-C₄H₉)Ia.4528 H n-C₃H₇ CH₂—CH═N—O(n-C₄H₉) Ia.4529 F n-C₃H₇ CH₂—CH═N—O(n-C₄H₉)Ia.4530 Cl n-C₃H₇ CH₂—CH═N—O(n-C₄H₉) Ia.4531 H n-C₄H₉ CH₂—CH═N—O(n-C₄H₉)Ia.4532 F n-C₄H₉ CH₂—CH═N—O(n-C₄H₉) Ia.4533 Cl n-C₄H₉ CH₂—CH═N—O(n-C₄H₉)Ia.4534 H CH₂—CH═CH₂ CH₂—CH═N—O(n-C₄H₉) Ia.4535 F CH₂—CH═CH₂CH₂—CH═N—O(n-C₄H₉) Ia.4536 Cl CH₂—CH═CH₂ CH₂—CH═N—O(n-C₄H₉) Ia.4537 HCH₂—C≡CH CH₂—CH═N—O(n-C₄H₉) Ia.4538 F CH₂—C≡CH CH₂—CH═N—O(n-C₄H₉)Ia.4539 Cl CH₂—C≡CH CH₂—CH═N—O(n-C₄H₉) Ia.4540 H CH₂—CO—OCH₃CH₂—CH═N—O(n-C₄H₉) Ia.4541 F CH₂—CO—OCH₃ CH₂—CH═N—O(n-C₄H₉) Ia.4542 ClCH₂—CO—OCH₃ CH₂—CH═N—O(n-C₄H₉) Ia.4543 H CH₂-phenyl CH₂—CH═N—O(n-C₄H₉₎Ia.4544 F CH₂-phenyl CH₂—CH═N—O(n-C₄H₉) Ia.4545 Cl CH₂-phenylCH₂—CH═N—O(n-C₄H₉) Ia.4546 H CH₃ CH₂—CH═N—OCH₂—CH═CH₂ Ia.4547 F CH₃CH₂—CH═N—OCH₂—CH═CH₂ Ia.4548 Cl CH₃ CH₂—CH═N—OCH₂—CH═CH₂ Ia.4549 H C₂H₅CH₂—CH═N—OCH₂—CH═CH₂ Ia.4550 F C₂H₅ CH₂—CH═N—OCH₂—CH═CH₂ Ia.4551 Cl C₂H₅CH₂—CH═N—OCH₂—CH═CH₂ Ia.4552 H n-C₃H₇ CH₂—CH═N—OCH₂—CH═CH₂ Ia.4553 Fn-C₃H₇ CH₂—CH═N—OCH₂—CH═CH₂ Ia.4554 Cl n-C₃H₇ CH₂—CH═N—OCH₂—CH═CH₂Ia.4555 H n-C₄H₉ CH₂—CH═N—OCH₂—CH═CH₂ Ia.4556 F n-C₄H₉CH₂—CH═N—OCH₂—CH═CH₂ Ia.4557 Cl n-C₄H₉ CH₂—CH═N—OCH₂—CH═CH₂ Ia.4558 HCH₂—CH═CH₂ CH₂—CH═N—OCH₂—CH═CH₂ Ia.4559 F CH₂—CH═CH₂CH₂—CH═N—OCH₂—CH═CH₂ Ia.4560 Cl CH₂—CH═CH₂ CH₂—CH═N—OCH₂—CH═CH₂ Ia.4561H CH₂—C≡CH CH₂—CH═N—OCH₂—CH═CH₂ Ia.4562 F CH₂—C≡CH CH₂—CH═N—OCH₂—CH═CH₂Ia.4563 Cl CH₂—C≡CH CH₂—CH═N—OCH₂—CH═CH₂ Ia.4564 H CH₂—CO—OCH₃CH₂—CH═N—OCH₂—CH═CH₂ Ia.4565 F CH₂—CO—OCH₃ CH₂—CH═N—OCH₂—CH═CH₂ Ia.4566Cl CH₂—CO—OCH₃ CH₂—CH═N—OCH₂—CH═CH₂ Ia.4567 H CH₂-phenylCH₂—CH═N—OCH₂—CH═CH₂ Ia.4568 F CH₂-phenyl CH₂—CH═N—OCH₂—CH═CH₂ Ia.4569Cl CH₂-phenyl CH₂—CH═N—OCH₂—CH═CH₂ Ia.4570 H CH₃ CH₂—COOH Ia.4571 F CH₃CH₂—COOH Ia.4572 Cl CH₃ CH₂—COOH Ia.4573 H C₂H₅ CH₂—COOH Ia.4574 F C₂H₅CH₂—COOH Ia.4575 Cl C₂H₅ CH₂—COOH Ia.4576 H n-C₃H₇ CH₂—COOH Ia.4577 Fn-C₃H₇ CH₂—COOH Ia.4578 Cl n-C₃H₇ CH₂—COOH Ia.4579 H n-C₄H₉ CH₂—COOHIa.4580 F n-C₄H₉ CH₂—COOH Ia.4581 Cl n-C₄H₉ CH₂—COOH Ia.4582 HCH₂—CH═CH₂ CH₂—COOH Ia.4583 F CH₂—CH═CH₂ CH₂—COOH Ia.4584 Cl CH₂—CH═CH₂CH₂—COOH Ia.4585 H CH₂—C≡CH CH₂—COOH Ia.4586 F CH₂—C≡CH CH₂—COOH Ia.4587Cl CH₂—C≡CH CH₂—COOH Ia.4588 H CH₂—CO—OCH₃ CH₂—COOH Ia.4589 FCH₂—CO—OCH₃ CH₂—COOH Ia.4590 Cl CH₂—CO—OCH₃ CH₂—COOH Ia.4591 HCH₂-phenyl CH₂—COOH Ia.4592 F CH₂-phenyl CH₂—COOH Ia.4593 Cl CH₂-phenylCH₂—COOH Ia.4594 H CH₃ CH(CH₃)—COOH Ia.4595 F CH₃ CH(CH₃)—COOH Ia.4596Cl CH₃ CH(CH₃)—COOH Ia.4597 H C₂H₅ CH(CH₃)—COOH Ia.4598 F C₂H₅CH(CH₃)—COOH Ia.4599 Cl C₂H₅ CH(CH₃)—COOH Ia.4600 H n-C₃H₇ CH(CH₃)—COOHIa.4601 F n-C₃H₇ CH(CH₃)—COOH Ia.4602 Cl n-C₃H₇ CH(CH₃)—COOH Ia.4603 Hn-C₄H₉ CH(CH₃)—COOH Ia.4604 F n-C₄H₉ CH(CH₃)—COOH Ia.4605 Cl n-C₄H₉CH(CH₃)—COOH Ia.4606 H CH₂—CH═CH₂ CH(CH₃)—COOH Ia.4607 F CH₂—CH═CH₂CH(CH₃)—COOH Ia.4608 Cl CH₂—CH═CH₂ CH(CH₃)—COOH Ia.4609 H CH₂—C≡CHCH(CH₃)—COOH Ia.4610 F CH₂—C≡CH CH(CH₃)—COOH Ia.4611 Cl CH₂—C≡CHCH(CH₃)—COOH Ia.4612 H CH₂—CO—OCH₃ CH(CH₃)—COOH Ia.4613 F CH₂—CO—OCH₃CH(CH₃)—COOH Ia.4614 Cl CH₂—CO—OCH₃ CH(CH₃)—COOH Ia.4615 H CH₂-phenylCH(CH₃)—COOH Ia.4616 F CH₂-phenyl CH(CH₃)—COOH Ia.4617 Cl CH₂-phenylCH(CH₃)—COOH Ia.4618 H CH₃ CH(C₂H₅)—COOH Ia.4619 F CH₃ CH(C₂H₅)—COOHIa.4620 Cl CH₃ CH(C₂H₅)—COOH Ia.4621 H C₂H₅ CH(C₂H₅)—COOH Ia.4622 F C₂H₅CH(C₂H₅)—COOH Ia.4623 Cl C₂H₅ CH(C₂H₅)—COOH Ia.4624 H n-C₃H₇CH(C₂H₅)—COOH Ia.4625 F n-C₃H₇ CH(C₂H₅)—COOH Ia.4626 Cl n-C₃H₇CH(C₂H₅)—COOH Ia.4627 H n-C₄H₉ CH(C₂H₅)—COOH Ia.4628 F n-C₄H₉CH(C₂H₅)—COOH Ia.4629 Cl n-C₄H₉ CH(C₂H₅)—COOH Ia.4630 H CH₂—CH═CH₂CH(C₂H₅)—COOH Ia.4631 F CH₂—CH═CH₂ CH(C₂H₅)—COOH Ia.4632 Cl CH₂—CH═CH₂CH(C₂H₅)—COOH Ia.4633 H CH₂—C≡CH CH(C₂H₅)—COOH Ia.4634 F CH₂—C≡CHCH(C₂H₅)—COOH Ia.4635 Cl CH₂—C≡CH CH(C₂H₅)—COOH Ia.4636 H CH₂—CO—OCH₃CH(C₂H₅)—COOH Ia.4637 F CH₂—CO—OCH₃ CH(C₂H₅)—COOH Ia.4638 Cl CH₂—CO—OCH₃CH(C₂H₅)—COOH Ia.4639 H CH₂-phenyl CH(C₂H₅)—COOH Ia.4640 F CH₂-phenylCH(C₂H₅)—COOH Ia.4641 Cl CH₂-phenyl CH(C₂H₅)—COOH Ia.4642 H CH₃CH₂—CO—OCH₃ Ia.4643 F CH₃ CH₂—CO—OCH₃ Ia.4644 Cl CH₃ CH₂—CO—OCH₃ Ia.4645H C₂H₅ CH₂—CO—OCH₃ Ia.4646 F C₂H₅ CH₂—CO—OCH₃ Ia.4647 Cl C₂H₅CH₂—CO—OCH₃ Ia.4648 H n-C₃H₇ CH₂—CO—OCH₃ Ia.4649 F n-C₃H₇ CH₂—CO—OCH₃Ia.4650 Cl n-C₃H₇ CH₂—CO—OCH₃ Ia.4651 H n-C₄H₉ CH₂—CO—OCH₃ Ia.4652 Fn-C₄H₉ CH₂—CO—OCH₃ Ia.4653 Cl n-C₄H₉ CH₂—CO—OCH₃ Ia.4654 H CH₃CH(CH₃)—CO—OCH₃ Ia.4655 F CH₃ CH(CH₃)—CO—OCH₃ Ia.4656 Cl CH₃CH(CH₃)—CO—OCH₃ Ia.4657 H C₂H₅ CH(CH₃)—CO—OCH₃ Ia.4658 F C₂H₅CH(CH₃)—CO—OCH₃ Ia.4659 Cl C₂H₅ CH(CH₃)—CO—OCH₃ Ia.4660 H n-C₃H₇CH(CH₃)—CO—OCH₃ Ia.4661 F n-C₃H₇ CH(CH₃)—CO—OCH₃ Ia.4662 Cl n-C₃H₇CH(CH₃)—CO—OCH₃ Ia.4663 H n-C₄H₉ CH(CH₃)—CO—OCH₃ Ia.4664 F n-C₄H₉CH(CH₃)—CO—OCH₃ Ia.4665 Cl n-C₄H₉ CH(CH₃)—CO—OCH₃ Ia.4666 H CH₂—CH═CH₂CH(CH₃)—CO—OCH₃ Ia.4667 F CH₂—CH═CH₂ CH(CH₃)—CO—OCH₃ Ia.4668 ClCH₂—CH═CH₂ CH(CH₃)—CO—OCH₃ Ia.4669 H CH₂—C≡CH CH(CH₃)—CO—OCH₃ Ia.4670 FCH₂—C≡CH CH(CH₃)—CO—OCH₃ Ia.4671 Cl CH₂—C≡CH CH(CH₃)—CO—OCH₃ Ia.4672 HCH₂—CO—OCH₃ CH(CH₃)—CO—OCH₃ Ia.4673 F CH₂—CO—OCH₃ CH(CH₃)—CO—OCH₃Ia.4674 Cl CH₂—CO—OCH₃ CH(CH₃)—CO—OCH₃ Ia.4675 H CH₂-phenylCH(CH₃)—CO—OCH₃ Ia.4676 F CH₂-phenyl CH(CH₃)—CO—OCH₃ Ia.4677 ClCH₂-phenyl CH(CH₃)—CO—OCH₃ Ia.4678 H CH₃ CH(C₂H₅)—CO—OCH₃ Ia.4679 F CH₃CH(C₂H₅)—CO—OCH₃ Ia.4680 Cl CH₃ CH(C₂H₅)—CO—OCH₃ Ia.4681 H C₂H₅CH(C₂H₅)—CO—OCH₃ Ia.4682 F C₂H₅ CH(C₂H₅)—CO—OCH₃ Ia.4683 Cl C₂H₅CH(C₂H₅)—CO—OCH₃ Ia.4684 H n-C₃H₇ CH(C₂H₅)—CO—OCH₃ Ia.4685 F n-C₃H₇CH(C₂H₅)—CO—OCH₃ Ia.4686 Cl n-C₃H₇ CH(C₂H₅)—CO—OCH₃ Ia.4687 H n-C₄H₉CH(C₂H₅)—CO—OCH₃ Ia.4688 F n-C₄H₉ CH(C₂H₅)—CO—OCH₃ Ia.4689 Cl n-C₄H₉CH(C₂H₅)—CO—OCH₃ Ia.4690 H CH₂—CH═CH₂ CH(C₂H₅)—CO—OCH₃ Ia.4691 FCH₂—CH═CH₂ CH(C₂H₅)—CO—OCH₃ Ia.4692 Cl CH₂—CH═CH₂ CH(C₂H₅)—CO—OCH₃Ia.4693 H CH₂—C≡CH CH(C₂H₅)—CO—OCH₃ Ia.4694 F CH₂—C≡CH CH(C₂H₅)—CO—OCH₃Ia.4695 Cl CH₂—C≡CH CH(C₂H₅)—CO—OCH₃ Ia.4696 H CH₂—CO—OCH₃CH(C₂H₅)—CO—OCH₃ Ia.4697 F CH₂—CO—OCH₃ CH(C₂H₅)—CO—OCH₃ Ia.4698 ClCH₂—CO—OCH₃ CH(C₂H₅)—CO—OCH₃ Ia.4699 H CH₂-phenyl CH(C₂H₅)—CO—OCH₃Ia.4700 F CH₂-phenyl CH(C₂H₅)—CO—OCH₃ Ia.4701 Cl CH₂-phenylCH(C₂H₅)—CO—OCH₃ Ia.4702 H CH₃ CH₂—CO—OC₂H₅ Ia.4703 F CH₃ CH₂—CO—OC₂H₅Ia.4704 Cl CH₃ CH₂—CO—OC₂H₅ Ia.4705 H C₂H₅ CH₂—CO—OC₂H₅ Ia.4706 F C₂H₅CH₂—CO—OC₂H₅ Ia.4707 Cl C₂H₅ CH₂—CO—OC₂H₅ Ia.4708 H n-C₃H₇ CH₂—CO—OC₂H₅Ia.4709 F n-C₃H₇ CH₂—CO—OC₂H₅ Ia.4710 Cl n-C₃H₇ CH₂—CO—OC₂H₅ Ia.4711 Hn-C₄H₉ CH₂—CO—OC₂H₅ Ia.4712 F n-C₄H₉ CH₂—CO—OC₂H₅ Ia.4713 Cl n-C₄H₉CH₂—CO—OC₂H₅ Ia.4714 H CH₂—CH═CH₂ CH₂—CO—OC₂H₅ Ia.4715 F CH₂—CH═CH₂CH₂—CO—OC₂H₅ Ia.4716 Cl CH₂—CH═CH₂ CH₂—CO—OC₂H₅ Ia.4717 H CH₂—C≡CHCH₂—CO—OC₂H₅ Ia.4718 F CH₂—C≡CH CH₂—CO—OC₂H₅ Ia.4719 Cl CH₂—C≡CHCH₂—CO—OC₂H₅ Ia.4720 H CH₂—CO—OCH₃ CH₂—CO—OC₂H₅ Ia.4721 F CH₂—CO—OCH₃CH₂—CO—OC₂H₅ Ia.4722 Cl CH₂—CO—OCH₃ CH₂—CO—OC₂H₅ Ia.4723 H CH₂-phenylCH₂—CO—OC₂H₅ Ia.4724 F CH₂-phenyl CH₂—CO—OC₂H₅ Ia.4725 Cl CH₂-phenylCH₂—CO—OC₂H₅ Ia.4726 H CH₃ CH(CH₃)—CO—OC₂H₅ Ia.4727 F CH₃CH(CH₃)—CO—OC₂H₅ Ia.4728 Cl CH₃ CH(CH₃)—CO—OC₂H₅ Ia.4729 H C₂H₅CH(CH₃)—CO—OC₂H₅ Ia.4730 F C₂H₅ CH(CH₃)—CO—OC₂H₅ Ia.4731 Cl C₂H₅CH(CH₃)—CO—OC₂H₅ Ia.4732 H n-C₃H₇ CH(CH₃)—CO—OC₂H₅ Ia.4733 F n-C₃H₇CH(CH₃)—CO—OC₂H₅ Ia.4734 Cl n-C₃H₇ CH(CH₃)—CO—OC₂H₅ Ia.4735 H n-C₄H₉CH(CH₃)—CO—OC₂H₅ Ia.4736 F n-C₄H₉ CH(CH₃)—CO—OC₂H₅ Ia.4737 Cl n-C₄H₉CH(CH₃)—CO—OC₂H₅ Ia.4738 H CH₂—CH═CH₂ CH(CH₃)—CO—OC₂H₅ Ia.4739 FCH₂—CH═CH₂ CH(CH₃)—CO—OC₂H₅ Ia.4740 Cl CH₂—CH═CH₂ CH(CH₃)—CO—OC₂H₅Ia.4741 H CH₂—C≡CH CH(CH₃)—CO—OC₂H₅ Ia.4742 F CH₂—C≡CH CH(CH₃)—CO—OC₂H₅Ia.4743 Cl CH₂—C≡CH CH(CH₃)—CO—OC₂H₅ Ia.4744 H CH₂—CO—OCH₃CH(CH₃)—CO—OC₂H₅ Ia.4745 F CH₂—CO—OCH₃ CH(CH₃)—CO—OC₂H₅ Ia.4746 ClCH₂—CO—OCH₃ CH(CH₃)—CO—OC₂H₅ Ia.4747 H CH₂-phenyl CH(CH₃)—CO—OC₂H₅Ia.4748 F CH₂-phenyl CH(CH₃)—CO—OC₂H₅ Ia.4749 Cl CH₂-phenylCH(CH₃)—CO—OC₂H₅ Ia.4750 H CH₃ CH(C₂H₅)—CO—OC₂H₅ Ia.4751 F CH₃CH(C₂H₅)—CO—OC₂H₅ Ia.4752 Cl CH₃ CH(C₂H₅)—CO—OC₂H₅ Ia.4753 H C₂H₅CH(C₂H₅)—CO—OC₂H₅ Ia.4754 F C₂H₅ CH(C₂H₅)—CO—OC₂H₅ Ia.4755 Cl C₂H₅CH(C₂H₅)—CO—OC₂H₅ Ia.4756 H n-C₃H₇ CH(C₂H₅)—CO—OC₂H₅ Ia.4757 F n-C₃H₇CH(C₂H₅)—CO—OC₂H₅ Ia.4758 Cl n-C₃H₇ CH(C₂H₅)—CO—OC₂H₅ Ia.4759 H n-C₄H₉CH(C₂H₅)—CO—OC₂H₅ Ia.4760 F n-C₄H₉ CH(C₂H₅)—CO—OC₂H₅ Ia.4761 Cl n-C₄H₉CH(C₂H₅)—CO—OC₂H₅ Ia.4762 H CH₂—CH═CH₂ CH(C₂H₅)—CO—OC₂H₅ Ia.4763 FCH₂—CH═CH₂ CH(C₂H₅)—CO—OC₂H₅ Ia.4764 Cl CH₂—CH═CH₂ CH(C₂H₅)—CO—OC₂H₅Ia.4765 H CH₂—C≡CH CH(C₂H₅)—CO—OC₂H₅ Ia.4766 F CH₂—C≡CHCH(C₂H₅)—CO—OC₂H₅ Ia.4767 Cl CH₂—C≡CH CH(C₂H₅)—CO—OC₂H₅ Ia.4768 HCH₂—CO—OCH₃ CH(C₂H₅)—CO—OC₂H₅ Ia.4769 F CH₂—CO—OCH₃ CH(C₂H₅)—CO—OC₂H₅Ia.4770 Cl CH₂—CO—OCH₃ CH(C₂H₅)—CO—OC₂H₅ Ia.4771 H CH₂-phenylCH(C₂H₅)—CO—OC₂H₅ Ia.4772 F CH₂-phenyl CH(C₂H₅)—CO—OC₂H₅ Ia.4773 ClCH₂-phenyl CH(C₂H₅)—CO—OC₂H₅ Ia.4774 H CH₃ CH₂—CO—OC(CH₃)₃ Ia.4775 F CH₃CH₂—CO—OC(CH₃)₃ Ia.4776 Cl CH₃ CH₂—CO—OC(CH₃)₃ Ia.4777 H C₂H₅CH₂—CO—OC(CH₃)₃ Ia.4778 F C₂H₅ CH₂—CO—OC(CH₃)₃ Ia.4779 Cl C₂H₅CH₂—CO—OC(CH₃)₃ Ia.4780 H n-C₃H₇ CH₂—CO—OC(CH₃)₃ Ia.4781 F n-C₃H₇CH₂—CO—OC(CH₃)₃ Ia.4782 Cl n-C₃H₇ CH₂—CO—OC(CH₃)₃ Ia.4783 H n-C₄H₉CH₂—CO—OC(CH₃)₃ Ia.4784 F n-C₄H₉ CH₂—CO—OC(CH₃)₃ Ia.4785 Cl n-C₄H₉CH₂—CO—OC(CH₃)₃ Ia.4786 H CH₂—CH═CH₂ CH₂—CO—OC(CH₃)₃ Ia.4787 FCH₂—CH═CH₂ CH₂—CO—OC(CH₃)₃ Ia.4788 Cl CH₂—CH═CH₂ CH₂—CO—OC(CH₃)₃ Ia.4789H CH₂—C≡CH CH₂—CO—OC(CH₃)₃ Ia.4790 F CH₂—C≡CH CH₂—CO—OC(CH₃)₃ Ia.4791 ClCH₂—C≡CH CH₂—CO—OC(CH₃)₃ Ia.4792 H CH₂—CO—OCH₃ CH₂—CO—OC(CH₃)₃ Ia.4793 FCH₂—CO—OCH₃ CH₂—CO—OC(CH₃)₃ Ia.4794 Cl CH₂—CO—OCH₃ CH₂—CO—OC(CH₃)₃Ia.4795 H CH₂-phenyl CH₂—CO—OC(CH₃)₃ Ia.4796 F CH₂-phenylCH₂—CO—OC(CH₃)₃ Ia.4797 Cl CH₂-phenyl CH₂—CO—OC(CH₃)₃ Ia.4798 H CH₃CH(CH₃)—CO—OC(CH₃)₃ Ia.4799 F CH₃ CH(CH₃)—CO—OC(CH₃)₃ Ia.4800 Cl CH₃CH(CH₃)—CO—OC(CH₃)₃ Ia.4801 H C₂H₅ CH(CH₃)—CO—OC(CH₃)₃ Ia.4802 F C₂H₅CH(CH₃)—CO—OC(CH₃)₃ Ia.4803 Cl C₂H₅ CH(CH₃)—CO—OC(CH₃)₃ Ia.4804 H n-C₃H₇CH(CH₃)—CO—OC(CH₃)₃ Ia.4805 F n-C₃H₇ CH(CH₃)—CO—OC(CH₃)₃ Ia.4806 Cln-C₃H₇ CH(CH₃)—CO—OC(CH₃)₃ Ia.4807 H n-C₄H₉ CH(CH₃)—CO—OC(CH₃)₃ Ia.4808F n-C₄H₉ CH(CH₃)—CO—OC(CH₃)₃ Ia.4809 Cl n-C₄H₉ CH(CH₃)—CO—OC(CH₃)₃Ia.4810 H CH₂—CH═CH₂ CH(CH₃)—CO—OC(CH₃)₃ Ia.4811 F CH₂—CH═CH₂CH(CH₃)—CO—OC(CH₃)₃ Ia.4812 Cl CH₂—CH═CH₂ CH(CH₃)—CO—OC(CH₃)₃ Ia.4813 HCH₂—C≡CH CH(CH₃)—CO—OC(CH₃)₃ Ia.4814 F CH₂—C≡CH CH(CH₃)—CO—OC(CH₃)₃Ia.4815 Cl CH₂—C≡CH CH(CH₃)—CO—OC(CH₃)₃ Ia.4816 H CH₂—CO—OCH₃CH(CH₃)—CO—OC(CH₃)₃ Ia.4817 F CH₂—CO—OCH₃ CH(CH₃)—CO—OC(CH₃)₃ Ia.4818 ClCH₂—CO—OCH₃ CH(CH₃)—CO—OC(CH₃)₃ Ia.4819 H CH₂-phenyl CH(CH₃)—CO—OC(CH₃)₃Ia.4820 F CH₂-phenyl CH(CH₃)—CO—OC(CH₃)₃ Ia.4821 Cl CH₂-phenylCH(CH₃)—CO—OC(CH₃)₃ Ia.4822 H CH₃ CH(C₂H₅)—CO—OC(CH₃)₃ Ia.4823 F CH₃CH(C₂H₅)—CO—OC(CH₃)₃ Ia.4824 Cl CH₃ CH(C₂H₅)—CO—OC(CH₃)₃ Ia.4825 H C₂H₅CH(C₂H₅)—CO—OC(CH₃)₃ Ia.4826 F C₂H₅ CH(C₂H₅)—CO—OC(CH₃)₃ Ia.4827 Cl C₂H₅CH(C₂H₅)—CO—OC(CH₃)₃ Ia.4828 H n-C₃H₇ CH(C₂H₅)—CO—OC(CH₃)₃ Ia.4829 Fn-C₃H₇ CH(C₂H₅)—CO—OC(CH₃)₃ Ia.4830 Cl n-C₃H₇ CH(C₂H₅)—CO—OC(CH₃)₃Ia.4831 H n-C₄H₉ CH(C₂H₅)—CO—OC(CH₃)₃ Ia.4832 F n-C₄H₉CH(C₂H₅)—CO—OC(CH₃)₃ Ia.4833 Cl n-C₄H₉ CH(C₂H₅)—CO—OC(CH₃)₃ Ia.4834 HCH₂—CH═CH₂ CH(C₂H₅)—CO—OC(CH₃)₃ Ia.4835 F CH₂—CH═CH₂CH(C₂H₅)—CO—OC(CH₃)₃ Ia.4836 Cl CH₂—CH═CH₂ CH(C₂H₅)—CO—OC(CH₃)₃ Ia.4837H CH₂—C≡CH CH(C₂H₅)—CO—OC(CH₃)₃ Ia.4838 F CH₂—C≡CH CH(C₂H₅)—CO—OC(CH₃)₃Ia.4839 Cl CH₂—C≡CH CH(C₂H₅)—CO—OC(CH₃)₃ Ia.4840 H CH₂—CO—OCH₃CH(C₂H₅)—CO—OC(CH₃)₃ Ia.4841 F CH₂—CO—OCH₃ CH(C₂H₅)—CO—OC(CH₃)₃ Ia.4842Cl CH₂—CO—OCH₃ CH(C₂H₅)—CO—OC(CH₃)₃ Ia.4843 H CH₂-phenylCH(C₂H₅)—CO—OC(CH₃)₃ Ia.4844 F CH₂-phenyl CH(C₂H₅)—CO—OC(CH₃)₃ Ia.4845Cl CH₂-phenyl CH(C₂H₅)—CO—OC(CH₃)₃ Ia.4846 H CH₃ CH₂—CO—SCH₃ Ia.4847 FCH₃ CH₂—CO—SCH₃ Ia.4848 Cl CH₃ CH₂—CO—SCH₃ Ia.4849 H C₂H₅ CH₂—CO—SCH₃Ia.4850 F C₂H₅ CH₂—CO—SCH₃ Ia.4851 Cl C₂H₅ CH₂—CO—SCH₃ Ia.4852 H n-C₃H₇CH₂—CO—SCH₃ Ia.4853 F n-C₃H₇ CH₂—CO—SCH₃ Ia.4854 Cl n-C₃H₇ CH₂—CO—SCH₃Ia.4855 H n-C₄H₉ CH₂—CO—SCH₃ Ia.4856 F n-C₄H₉ CH₂—CO—SCH₃ Ia.4857 Cln-C₄H₉ CH₂—CO—SCH₃ Ia.4858 H CH₂—CH═CH₂ CH₂—CO—SCH₃ Ia.4859 F CH₂—CH═CH₂CH₂—CO—SCH₃ Ia.4860 Cl CH₂—CH═CH₂ CH₂—CO—SCH₃ Ia.4861 H CH₂—C≡CHCH₂—CO—SCH₃ Ia.4862 F CH₂—C≡CH CH₂—CO—SCH₃ Ia.4863 Cl CH₂—C≡CHCH₂—CO—SCH₃ Ia.4864 H CH₂—CO—OCH₃ CH₂—CO—SCH₃ Ia.4865 F CH₂—CO—OCH₃CH₂—CO—SCH₃ Ia.4866 Cl CH₂—CO—OCH₃ CH₂—CO—SCH₃ Ia.4867 H CH₂-phenylCH₂—CO—SCH₃ Ia.4868 F CH₂-phenyl CH₂—CO—SCH₃ Ia.4869 Cl CH₂-phenylCH₂—CO—SCH₃ Ia.4870 H CH₃ CH₂—CO—N(CH₃)₂ Ia.4871 F CH₃ CH₂—CO—N(CH₃)₂Ia.4872 Cl CH₃ CH₂—CO—N(CH₃)₂ Ia.4873 H C₂H₅ CH₂—CO—N(CH₃)₂ Ia.4874 FC₂H₅ CH₂—CO—N(CH₃)₂ Ia.4875 Cl C₂H₅ CH₂—CO—N(CH₃)₂ Ia.4876 H n-C₃H₇CH₂—CO—N(CH₃)₂ Ia.4877 F n-C₃H₇ CH₂—CO—N(CH₃)₂ Ia.4878 Cl n-C₃H₇CH₂—CO—N(CH₃)₂ Ia.4879 H n-C₄H₉ CH₂—CO—N(CH₃)₂ Ia.4880 F n-C₄H₉CH₂—CO—N(CH₃)₂ Ia.4881 Cl n-C₄H₉ CH₂—CO—N(CH₃)₂ Ia.4882 H CH₂—CH═CH₂CH₂—CO—N(CH₃)₂ Ia.4883 F CH₂—CH═CH₂ CH₂—CO—N(CH₃)₂ Ia.4884 Cl CH₂—CH═CH₂CH₂—CO—N(CH₃)₂ Ia.4885 H CH₂—C≡CH CH₂—CO—N(CH₃)₂ Ia.4886 F CH₂—C≡CHCH₂—CO—N(CH₃)₂ Ia.4887 Cl CH₂—C≡CH CH₂—CO—N(CH₃)₂ Ia.4888 H CH₂—CO—OCH₃CH₂—CO—N(CH₃)₂ Ia.4889 F CH₂—CO—OCH₃ CH₂—CO—N(CH₃)₂ Ia.4890 ClCH₂—CO—OCH₃ CH₂—CO—N(CH₃)₂ Ia.4891 H CH₂-phenyl CH₂—CO—N(CH₃)₂ Ia.4892 FCH₂-phenyl CH₂—CO—N(CH₃)₂ Ia.4893 Cl CH₂-phenyl CH₂—CO—N(CH₃)₂ Ia.4894 HCH₃ CH(CH₃)—CO—N(CH₃)₂ Ia.4895 F CH₃ CH(CH₃)—CO—N(CH₃)₂ Ia.4896 Cl CH₃CH(CH₃)—CO—N(CH₃)₂ Ia.4897 H C₂H₅ CH(CH₃)—CO—N(CH₃)₂ Ia.4898 F C₂H₅CH(CH₃)—CO—N(CH₃)₂ Ia.4899 Cl C₂H₅ CH(CH₃)—CO—N(CH₃)₂ Ia.4900 H n-C₃H₇CH(CH₃)—CO—N(CH₃)₂ Ia.4901 F n-C₃H₇ CH(CH₃)—CO—N(CH₃)₂ Ia.4902 Cl n-C₃H₇CH(CH₃)—CO—N(CH₃)₂ Ia.4903 H n-C₄H₉ CH(CH₃)—CO—N(CH₃)₂ Ia.4904 F n-C₄H₉CH(CH₃)—CO—N(CH₃)₂ Ia.4905 Cl n-C₄H₉ CH(CH₃)—CO—N(CH₃)₂ Ia.4906 HCH₂—CH═CH₂ CH(CH₃)—CO—N(CH₃)₂ Ia.4907 F CH₂—CH═CH₂ CH(CH₃)—CO—N(CH₃)₂Ia.4908 Cl CH₂—CH═CH₂ CH(CH₃)—CO—N(CH₃)₂ Ia.4909 H CH₂—C≡CHCH(CH₃)—CO—N(CH₃)₂ Ia.4910 F CH₂—C≡CH CH(CH₃)—CO—N(CH₃)₂ Ia.4911 ClCH₂—C≡CH CH(CH₃)—CO—N(CH₃)₂ Ia.4912 H CH₂—CO—OCH₃ CH(CH₃)—CO—N(CH₃)₂Ia.4913 F CH₂—CO—OCH₃ CH(CH₃)—CO—N(CH₃)₂ Ia.4914 Cl CH₂—CO—OCH₃CH(CH₃)—CO—N(CH₃)₂ Ia.4915 H CH₂-phenyl CH(CH₃)—CO—N(CH₃)₂ Ia.4916 FCH₂-phenyl CH(CH₃)—CO—N(CH₃)₂ Ia.4917 Cl CH₂-phenyl CH(CH₃)—CO—N(CH₃)₂Ia.4918 H CH₃ CH(C₂H₅)—CO—N(CH₃)₂ Ia.4919 F CH₃ CH(C₂H₅)—CO—N(CH₃)₂Ia.4920 Cl CH₃ CH(C₂H₅)—CO—N(CH₃)₂ Ia.4921 H C₂H₅ CH(C₂H₅)—CO—N(CH₃)₂Ia.4922 F C₂H₅ CH(C₂H₅)—CO—N(CH₃)₂ Ia.4923 Cl C₂H₅ CH(C₂H₅)—CO—N(CH₃)₂Ia.4924 H n-C₃H₇ CH(C₂H₅)—CO—N(CH₃)₂ Ia.4925 F n-C₃H₇CH(C₂H₅)—CO—N(CH₃)₂ Ia.4926 Cl n-C₃H₇ CH(C₂H₅)—CO—N(CH₃)₂ Ia.4927 Hn-C₄H₉ CH(C₂H₅)—CO—N(CH₃)₂ Ia.4928 F n-C₄H₉ CH(C₂H₅)—CO—N(CH₃)₂ Ia.4929Cl n-C₄H₉ CH(C₂H₅)—CO—N(CH₃)₂ Ia.4930 H CH₂—CH═CH₂ CH(C₂H₅)—CO—N(CH₃)₂Ia.4931 F CH₂—CH═CH₂ CH(C₂H₅)—CO—N(CH₃)₂ Ia.4932 Cl CH₂—CH═CH₂CH(C₂H₅)—CO—N(CH₃)₂ Ia.4933 H CH₂—C≡CH CH(C₂H₅)—CO—N(CH₃)₂ Ia.4934 FCH₂—C≡CH CH(C₂H₅)—CO—N(CH₃)₂ Ia.4935 Cl CH₂—C≡CH CH(C₂H₅)—CO—N(CH₃)₂Ia.4936 H CH₂—CO—OCH₃ CH(C₂H₅)—CO—N(CH₃)₂ Ia.4937 F CH₂—CO—OCH₃CH(C₂H₅)—CO—N(CH₃)₂ Ia.4938 Cl CH₂—CO—OCH₃ CH(C₂H₅)—CO—N(CH₃)₂ Ia.4939 HCH₂-phenyl CH(C₂H₅)—CO—N(CH₃)₂ Ia.4940 F CH₂-phenyl CH(C₂H₅)—CO—N(CH₃)₂Ia.4941 Cl CH₂-phenyl CH(C₂H₅)—CO—N(CH₃)₂ Ia.4942 H CH₃ cyclopentylIa.4943 F CH₃ cyclopentyl Ia.4944 Cl CH₃ cyclopentyl Ia.4945 H C₂H₅cyclopentyl Ia.4946 F C₂H₅ cyclopentyl Ia.4947 Cl C₂H₅ cyclopentylIa.4948 H n-C₃H₇ cyclopentyl Ia.4949 F n-C₃H₇ cyclopentyl Ia.4950 Cln-C₃H₇ cyclopentyl Ia.4951 H n-C₄H₉ cyclopentyl Ia.4952 F n-C₄H₉cyclopentyl Ia.4953 Cl n-C₄H₉ cyclopentyl Ia.4954 H CH₂—CH═CH₂cyclopentyl Ia.4955 F CH₂—CH═CH₂ cyclopentyl Ia.4956 Cl CH₂—CH═CH₂cyclopentyl Ia.4957 H CH₂—C≡CH cyclopentyl Ia.4958 F CH₂—C≡CHcyclopentyl Ia.4959 Cl CH₂—C≡CH cyclopentyl Ia.4960 H CH₂—CO—OCH₃cyclopentyl Ia.4961 F CH₂—CO—OCH₃ cyclopentyl Ia.4962 Cl CH₂—CO—OCH₃cyclopentyl Ia.4963 H CH₂-phenyl cyclopentyl Ia.4964 F CH₂-phenylcyclopentyl Ia.4965 Cl CH₂-phenyl cyclopentyl Ia.4966 H CH₃ cyclohexylIa.4967 F CH₃ cyclohexyl Ia.4968 Cl CH₃ cyclohexyl Ia.4969 H C₂H₅cyclohexyl Ia.4970 F C₂H₅ cyclohexyl Ia.4971 Cl C₂H₅ cyclohexyl Ia.4972H n-C₃H₇ cyclohexyl Ia.4973 F n-C₃H₇ cyclohexyl Ia.4974 Cl n-C₃H₇cyclohexyl Ia.4975 H n-C₄H₉ cyclohexyl Ia.4976 F n-C₄H₉ cyclohexylIa.4977 Cl n-C₄H₉ cyclohexyl Ia.4978 H CH₂—CH═CH₂ cyclohexyl Ia.4979 FCH₂—CH═CH₂ cyclohexyl Ia.4980 Cl CH₂—CH═CH₂ cyclohexyl Ia.4981 HCH₂—C≡CH cyclohexyl Ia.4982 F CH₂—C≡CH cyclohexyl Ia.4983 Cl CH₂—C≡CHcyclohexyl Ia.4984 H CH₂—CO—OCH₃ cyclohexyl Ia.4985 F CH₂—CO—OCH₃cyclohexyl Ia.4986 Cl CH₂—CO—OCH₃ cyclohexyl Ia.4987 H CH₂-phenylcyclohexyl Ia.4988 F CH₂-phenyl cyclohexyl Ia.4989 Cl CH₂-phenylcyclohexyl Ia.4990 H CH₃ phenyl Ia.4991 F CH₃ phenyl Ia.4992 Cl CH₃phenyl Ia.4993 H C₂H₅ phenyl Ia.4994 F C₂H₅ phenyl Ia.4995 Cl C₂H₅phenyl Ia.4996 H n-C₃H₇ phenyl Ia.4997 F n-C₃H₇ phenyl Ia.4998 Cl n-C₃H₇phenyl Ia.4999 H n-C₄H₉ phenyl Ia.5000 F n-C₄H₉ phenyl Ia.5001 Cl n-C₄H₉phenyl Ia.5002 H CH₂—CH═CH₂ phenyl Ia.5003 F CH₂—CH═CH₂ phenyl Ia.5004Cl CH₂—CH═CH₂ phenyl Ia.5005 H CH₂—C≡CH phenyl Ia.5006 F CH₂—C≡CH phenylIa.5007 Cl CH₂—C≡CH phenyl Ia.5008 H CH₂—CO—OCH₃ phenyl Ia.5009 FCH₂—CO—OCH₃ phenyl Ia.5010 Cl CH₂—CO—OCH₃ phenyl Ia.5011 H CH₂-phenylphenyl Ia.5012 F CH₂-phenyl phenyl Ia.5013 Cl CH₂-phenyl phenyl Ia.5014H CH₃ CH₂-cyclopentyl Ia.5015 F CH₃ CH₂-cyclopentyl Ia.5016 Cl CH₃CH₂-cyclopentyl Ia.5017 H C₂H₅ CH₂-cyclopentyl Ia.5018 F C₂H₅CH₂-cyclopentyl Ia.5019 Cl C₂H₅ CH₂-cyclopentyl Ia.5020 H n-C₃H₇CH₂-cyclopentyl Ia.5021 F n-C₃H₇ CH₂-cyclopentyl Ia.5022 Cl n-C₃H₇CH₂-cyclopentyl Ia.5023 H n-C₄H₉ CH₂-cyclopentyl Ia.5024 F n-C₄H₉CH₂-cyclopentyl Ia.5025 Cl n-C₄H₉ CH₂-cyclopentyl Ia.5026 H CH₂—CH═CH₂CH₂-cyclopentyl Ia.5027 F CH₂—CH═CH₂ CH₂-cyclopentyl Ia.5028 ClCH₂—CH═CH₂ CH₂-cyclopentyl Ia.5029 H CH₂—C≡CH CH₂-cyclopentyl Ia.5030 FCH₂—C≡CH CH₂-cyclopentyl Ia.5031 Cl CH₂—C≡CH CH₂-cyclopentyl Ia.5032 HCH₂—CO—OCH₃ CH₂-cyclopentyl Ia.5033 F CH₂—CO—OCH₃ CH₂-cyclopentylIa.5034 Cl CH₂—CO—OCH₃ CH₂-cyclopentyl Ia.5035 H CH₂-phenylCH₂-cyclopentyl Ia.5036 F CH₂-phenyl CH₂-cyclopentyl Ia.5037 ClCH₂-phenyl CH₂-cyclopentyl Ia.5038 H CH₃ CH₂-cyclohexyl Ia.5039 F CH₃CH₂-cyclohexyl Ia.5040 Cl CH₃ CH₂-cyclohexyl Ia.5041 H C₂H₅CH₂-cyclohexyl Ia.5042 F C₂H₅ CH₂-cyclohexyl Ia.5043 Cl C₂H₅CH₂-cyclohexyl Ia.5044 H n-C₃H₇ CH₂-cyclohexyl Ia.5045 F n-C₃H₇CH₂-cyclohexyl Ia.5046 Cl n-C₃H₇ CH₂-cyclohexyl Ia.5047 H n-C₄H₉CH₂-cyclohexyl Ia.5048 F n-C₄H₉ CH₂-cyclohexyl Ia.5049 Cl n-C₄H₉CH₂-cyclohexyl Ia.5050 H CH₂—CH═CH₂ CH₂-cyclohexyl Ia.5051 F CH₂—CH═CH₂CH₂-cyclohexyl Ia.5052 Cl CH₂—CH═CH₂ CH₂-cyclohexyl Ia.5053 H CH₂—C≡CHCH₂-cyclohexyl Ia.5054 F CH₂—C≡CH CH₂-cyclohexyl Ia.5055 Cl CH₂—C≡CHCH₂-cyclohexyl Ia.5056 H CH₂—CO—OCH₃ CH₂-cyclohexyl Ia.5057 FCH₂—CO—OCH₃ CH₂-cyclohexyl Ia.5058 Cl CH₂—CO—OCH₃ CH₂-cyclohexyl Ia.5059H CH₂-phenyl CH₂-cyclohexyl Ia.5060 F CH₂-phenyl CH₂-cyclohexyl Ia.5061Cl CH₂-phenyl CH₂-cyclohexyl Ia.5062 H CH₃ CH₂-phenyl Ia.5063 F CH₃CH₂-phenyl Ia.5064 Cl CH₃ CH₂-phenyl Ia.5065 H C₂H₅ CH₂-phenyl Ia.5066 FC₂H₅ CH₂-phenyl Ia.5067 Cl C₂H₅ CH₂-phenyl Ia.5068 H n-C₃H₇ CH₂-phenylIa.5069 F n-C₃H₇ CH₂-phenyl Ia.5070 Cl n-C₃H₇ CH₂-phenyl Ia.5071 Hn-C₄H₉ CH₂-phenyl Ia.5072 F n-C₄H₉ CH₂-phenyl Ia.5073 Cl n-C₄H₉CH₂-phenyl Ia.5074 H CH₃ CH₂-(oxiran-2-yl) Ia.5075 F CH₃CH₂-(oxiran-2-yl) Ia.5076 Cl CH₃ CH₂-(oxiran-2-yl) Ia.5077 H C₂H₅CH₂-(oxiran-2-yl) Ia.5078 F C₂H₅ CH₂-(oxiran-2-yl) Ia.5079 Cl C₂H₅CH₂-(oxiran-2-yl) Ia.5080 H n-C₃H₇ CH₂-(oxiran-2-yl) Ia.5081 F n-C₃H₇CH₂-(oxiran-2-yl) Ia.5082 Cl n-C₃H₇ CH₂-(oxiran-2-yl) Ia.5083 H n-C₄H₉CH₂-(oxiran-2-yl) Ia.5084 F n-C₄H₉ CH₂-(oxiran-2-yl) Ia.5085 Cl n-C₄H₉CH₂-(oxiran-2-yl) Ia.5086 H CH₂—CH═CH₂ CH₂-(oxiran-2-yl) Ia.5087 FCH₂—CH═CH₂ CH₂-(oxiran-2-yl) Ia.5088 Cl CH₂—CH═CH₂ CH₂-(oxiran-2-yl)Ia.5089 H CH₂—C≡CH CH₂-(oxiran-2-yl) Ia.5090 F CH₂—C≡CHCH₂-(oxiran-2-yl) Ia.5091 Cl CH₂—C≡CH CH₂-(oxiran-2-yl) Ia.5092 HCH₂—CO—OCH₃ CH₂-(oxiran-2-yl) Ia.5093 F CH₂—CO—OCH₃ CH₂-(oxiran-2-yl)Ia.5094 Cl CH₂—CO—OCH₃ CH₂-(oxiran-2-yl) Ia.5095 H CH₂-phenylCH₂-(oxiran-2-yl) Ia.5096 F CH₂-phenyl CH₂-(oxiran-2-yl) Ia.5097 ClCH₂-phenyl CH₂-(oxiran-2-yl) Ia.5098 H CH₃ CH₂-(oxetan-3-yl) Ia.5099 FCH₃ CH₂-(oxetan-3-yl) Ia.5100 Cl CH₃ CH₂-(oxetan-3-yl) Ia.5101 H C₂H₅CH₂-(oxetan-3-yl) Ia.5102 F C₂H₅ CH₂-(oxetan-3-yl) Ia.5103 Cl C₂H₅CH₂-(oxetan-3-yl) Ia.5104 H n-C₃H₇ CH₂-(oxetan-3-yl) Ia.5105 F n-C₃H₇CH₂-(oxetan-3-yl) Ia.5106 Cl n-C₃H₇ CH₂-(oxetan-3-yl) Ia.5107 H n-C₄H₉CH₂-(oxetan-3-yl) Ia.5108 F n-C₄H₉ CH₂-(oxetan-3-yl) Ia.5109 Cl n-C₄H₉CH₂-(oxetan-3-yl) Ia.5110 H CH₂—CH═CH₂ CH₂-(oxetan-3-yl) Ia.5111 FCH₂—CH═CH₂ CH₂-(oxetan-3-yl) Ia.5112 Cl CH₂—CH═CH₂ CH₂-(oxetan-3-yl)Ia.5113 H CH₂—C≡CH CH₂-(oxetan-3-yl) Ia.5114 F CH₂—C≡CHCH₂-(oxetan-3-yl) Ia.5115 Cl CH₂—C≡CH CH₂-(oxetan-3-yl) Ia.5116 HCH₂—CO—OCH₃ CH₂-(oxetan-3-yl) Ia.5117 F CH₂—CO—OCH₃ CH₂-(oxetan-3-yl)Ia.5118 Cl CH₂—CO—OCH₃ CH₂-(oxetan-3-yl) Ia.5119 H CH₂-phenylCH₂-(oxetan-3-yl) Ia.5120 F CH₂-phenyl CH₂-(oxetan-3-yl) Ia.5121 ClCH₂-phenyl CH₂-(oxetan-3-yl) Ia.5122 H CH₃ CH₂—CH₂-(pyrrolidin-1-yl)Ia.5123 F CH₃ CH₂—CH₂-(pyrrolidin-1-yl) Ia.5124 Cl CH₃CH₂—CH₂-(pyrrolidin-1-yl) Ia.5125 H C₂H₅ CH₂—CH₂-(pyrrolidin-1-yl)Ia.5126 F C₂H₅ CH₂—CH₂-(pyrrolidin-1-yl) Ia.5127 Cl C₂H₅CH₂—CH₂-(pyrrolidin-1-yl) Ia.5128 H n-C₃H₇ CH₂—CH₂-(pyrrolidin-1-yl)Ia.5129 F n-C₃H₇ CH₂—CH₂-(pyrrolidin-1-yl) Ia.5130 Cl n-C₃H₇CH₂—CH₂-(pyrrolidin-1-yl) Ia.5131 H n-C₄H₉ CH₂—CH₂-(pyrrolidin-1-yl)Ia.5132 F n-C₄H₉ CH₂—CH₂-(pyrrolidin-1-yl) Ia.5133 Cl n-C₄H₉CH₂—CH₂-(pyrrolidin-1-yl) Ia.5134 H CH₂—CH═CH₂ CH₂—CH₂-(pyrrolidin-1-yl)Ia.5135 F CH₂—CH═CH₂ CH₂—CH₂-(pyrrolidin-1-yl) Ia.5136 Cl CH₂—CH═CH₂CH₂—CH₂-(pyrrolidin-1-yl) Ia.5137 H CH₂—C≡CH CH₂—CH₂-(pyrrolidin-1-yl)Ia.5138 F CH₂—C≡CH CH₂—CH₂-(pyrrolidin-1-yl) Ia.5139 Cl CH₂—C≡CHCH₂—CH₂-(pyrrolidin-1-yl) Ia.5140 H CH₂—CO—OCH₃CH₂—CH₂-(pyrrolidin-1-yl) Ia.5141 F CH₂—CO—OCH₃CH₂—CH₂-(pyrrolidin-1-yl) Ia.5142 Cl CH₂—CO—OCH₃CH₂—CH₂-(pyrrolidin-1-yl) Ia.5143 H CH₂-phenyl CH₂—CH₂-(pyrrolidin-1-yl)Ia.5144 F CH₂-phenyl CH₂—CH₂-(pyrrolidin-1-yl) Ia.5145 Cl CH₂-phenylCH₂—CH₂-(pyrrolidin-1-yl) Ia.5146 H CH₃ CH₂-(pyridin-2-yl) Ia.5147 F CH₃CH₂-(pyridin-2-yl) Ia.5148 Cl CH₃ CH₂-(pyridin-2-yl) Ia.5149 H C₂H₅CH₂-(pyridin-2-yl) Ia.5150 F C₂H₅ CH₂-(pyridin-2-yl) Ia.5151 Cl C₂H₅CH₂-(pyridin-2-yl) Ia.5152 H n-C₃H₇ CH₂-(pyridin-2-yl) Ia.5153 F n-C₃H₇CH₂-(pyridin-2-yl) Ia.5154 Cl n-C₃H₇ CH₂-(pyridin-2-yl) Ia.5155 H n-C₄H₉CH₂-(pyridin-2-yl) Ia.5156 F n-C₄H₉ CH₂-(pyridin-2-yl) Ia.5157 Cl n-C₄H₉CH₂-(pyridin-2-yl) Ia.5158 H CH₂—CH═CH₂ CH₂-(pyridin-2-yl) Ia.5159 FCH₂—CH═CH₂ CH₂-(pyridin-2-yl) Ia.5160 Cl CH₂—CH═CH₂ CH₂-(pyridin-2-yl)Ia.5161 H CH₂—C≡CH CH₂-(pyridin-2-yl) Ia.5162 F CH₂—C≡CHCH₂-(pyridin-2-yl) Ia.5163 Cl CH₂—C≡CH CH₂-(pyridin-2-yl) Ia.5164 HCH₂—CO—OCH₃ CH₂-(pyridin-2-yl) Ia.5165 F CH₂—CO—OCH₃ CH₂-(pyridin-2-yl)Ia.5166 Cl CH₂—CO—OCH₃ CH₂-(pyridin-2-yl) Ia.5167 H CH₂-phenylCH₂-(pyridin-2-yl) Ia.5168 F CH₂-phenyl CH₂-(pyridin-2-yl) Ia.5169 ClCH₂-phenyl CH₂-(pyridin-2-yl)

Furthermore, very especially preferred are the substituted3-phenylpyrazoles of the formulae Ib to Iu below, in particular

the compounds Ib.1-Ib.3060, which differ from the correspondingcompounds Ia.1-Ia.3060 only by the fact that R³ is fluorine:

the compounds Ic.1-Ic.3060, which differ from the correspondingcompounds Ia.1-Ia. 3060 only by the fact that R³ is trifluoromethyl:

the compounds Id.1-Id.3060, which differ form the correspondingcompounds Ia.1-Ia.3060 only by the fact that R² is trifluoromethyl andR³ is fluorine:

the compounds Ie.1-Ie.3060, which differ form the correspondingcompounds Ia.1-Ia.3060 only by the fact that R² is methylsulfonyl:

the compounds If.1-If.3060, which differ from the correspondingcompounds Ia.1-Ia.3060 only by the fact that R² is methylsulfonyl and R³is fluorine:

the compounds Ig.1-Ig.3060, which differ from the correspondingcompounds Ia.1-Ia.3060 only by the fact that X is the group —CH═C(Cl)—:

the compounds Ih.1-Ih.3060, which differ from the correspondingcompounds Ia.1-Ia.3060 only by the fact that X is the group —CH═C(Cl)—and R³ is fluorine:

the compounds Ik.1-Ik.3060, which differ from the correspondingcompounds Ia.1-Ia.3060 only by the fact that X is the group —CH═C(Cl)—and R² is trifluoromethyl:

the compounds Im.1-Im.3060, which differ from the correspondingcompounds Ia.1-Ia.3060 only by the fact that X is the group —CH═C(Cl)—,R² is trifluoromethyl and R³ is

the compounds In.1-In. 3060, which differ from the correspondingcompounds Ia.1-Ia.3060 only the fact that X is the group —CH═C(Cl)— andR² is methylsulfonyl:

the compounds Io.1-Io.3060, which differ from the correspondingcompounds Ia.1-Ia.3060 only by the fact that X is the group —CH═C(Cl)—,R² is methylsulfonyl and R³ is fluorine:

the compounds Ip.1-Ip.3060, which differ from the correspondingcompounds Ia.1-Ia.3060 only by the fact that X is the 1,2-ethynediylgroup:

the compounds Iq.1-Iq.3060, which differ from the correspondingcompounds Ia.1-Ia.3060 only by the fact that X is the 1,2-ethynediylgroup and R³ is fluorine:

the compounds Ir.1-Ir.3060, which differ from the correspondingcompounds Ia.1-Ia.3060 only by the fact that X is the 1,2-ethynediylgroup and R² is trifluoromethyl:

the compounds Is.1-Is.3060, which differ from the correspondingcompounds Ia.1-Ia.3060 only by the fact that X is the 1,2-ethynediylgroup, R² is trifluoromethyl and R³ is fluorine:

the compounds It.1-It.3060, which differ from the correspondingcompounds Ia.1-Ia.3060 only by the fact that X is the 1,2-ethynediylgroup and R² is methylsulfonyl:

the compounds Iu.1-Iu.3060, which differ from the correspondingcompounds Ia.1-Ia.3060 only by the fact that X is the 1,2-ethynediylgroup, R² is methylsulfonyl and R³ is fluorine:

The substituted 3-phenylpyrazoles of the formula I are accessible invarious ways, in particular by one of the processes below:

A) conversion of a 3-pyrazolylphenylcarboxylic acid II into thecorresponding alkoxyamide III followed by alkylation or acylation in amanner known per se {see, for example, Houben-Weyl, Methoden derorganischen Chemie [Methods in organic chemistry], Vol. E5, Georg ThiemeVerlag, Stuttgart 1985, p. 587 et seq., 826 et seq. and 1141 et seq.}:

L is a customary leaving group, such as halogen, methylsulfonyloxy,trifluoromethylsulfonyloxy or p-tolylsulfonyloxy.

The conversion of II into III can be effected in two ways:

One embodiment consists in first preparing, form II, the correspondingacid chloride and then reacting the latter with an alkxoyamine H₂N—OR⁷in the presence of a base—eg. an amine such as triethylamine orpyridine, an alkali metal carbonate such as potassium carbonate, analkali metal hydride such as sodium hydride or an alkali metal hydroxidesuch as sodium hydroxide and potassium hydroxide.

Examples of suitable chlorinating agents are phosgene, oxalyl chloride,phosphorus oxychloride and thionyl chloride. As a rule, the chlorinationis effected in an inert organic solvent, suitable substances being, forexample, aliphatic or aromatic hydrocarbons such as n-hexane andtoluene, halo-hydrocarbons such as dichloromethane, ethers such asdiethyl ether and tetrahydrofuran, and aprotic solvents such asdimethylformamide and acetonitrile.

In general, the abovementioned solvents and mixtures of these with waterare generally also suitable for reacting the acid chloride with H₂N—OR⁷.

A second embodiment consists in reacting II directly with thealkoxyamine H₂N—OR⁷ in one of the organic solvents mentioned above. Theprocess is preferably carried out in the presence of a coupling reagent,such as carbonyldiimidazole and dicyclohexylcarbodiimide.

The alkoxyamide III is subsequently alkylated or acylated with analkylating, or acylating, agent L-R⁶. The process is normally carriedout in the presence of a base, eg. an amine such as triethylamine andpyridine, an alkali metal carbonate such as potassium carbonate, analkali metal hydride such as sodium hydride or an alkali metal hydroxidesuch as sodium hydroxide and potassium hydroxide.

Examples of suitable solvents are aliphatic or aromatic hydrocarbonssuch as n-hexane and toluene, halohydrocarbons such as dichloromethane,ethers such as diethyl ether and tetrahydrofuran, aprotic solvents suchas dimethylformamide and acetonitrile, and mixtures of these.

The reaction may give the isomer IV as a secondary product; it can beremoved in the customary manner, eg. by means of extraction,crystallization, distillation, or chromatography.

All the abovementioned reactions are carried out between the melting andthe boiling point of the solvent, in particular at from 0° to 100° C.The reactants are preferably employed in approximate equimolar amountsor in an excess of approximately up to ten times the molar amount, basedon the amount of carboxylic acid II, its acid chloride or the alkoxyamide III.

B) Wittig reaction of a 3-pyrazolylbenzaldehyde V with an ylide VI or aphosphonate VII in the presence of a base {cf., for examples,Houben-Weyl, Methoden der organischen Chemie [Methods in organicchemistry], Vol. 5/lb, Georg Thieme Verlag, Stuttgart 1972, p. 383 etseq.}:

Ph represents the substituents on the phosphorus which areconventionally used in Wittig reagents, in particular phenyl; R^(a) is,in particular, lower alkyl such as methyl or ethyl.

The reaction with VII is generally carried out in the presence of abase, eg. an alkali metal hydride such as sodium hydride, an alkalimetal hydroxide such as sodium hydroxide and potassium hydroxide, analkoxide such as potassium tertbutoxide, or butyllithium.

Examples of suitable solvents are aliphatic or aromatic hydrocarbonssuch as n-hexane and toluene, halohydrocarbons such as dichloromethane,ethers such as diethyl ether and tetrahydrofuran, aprotic solvents suchas dimethylformamide and acetonitrile.

The reaction temperature is normally between the melting and boilingpoint of the reaction mixture, preferably at from 0° to 100° C.

Base and reactant VI or VII are generally employed in approximateequimolar amounts or in an excess of up to approximately ten times themolar amount, based on the amount of V.

Other possibilities for the preparation of various compounds I from the3-pyrazolylbenzaldehydes V include the aldol condensation reaction whichis known per se {conditions suitable for this purpose can be found in,for example, Nielsen, Org. React. 16 (1968), 1 et seq.}, and Knoevenagelor Perkin condensation reactions. Suitable reaction conditions aredescribed, for example, in Org. React. 15 (1967), 204 et seq. {method ofKnoevenagel} and Johnson, Org. React. 1 (1942), 210 et seq. {method ofPerkin}.

C) Diazotization of a 3-pyrazolylaniline VIII and arylation of theresulting diazonium compound by the method of Meerwein {see, in thiscontext, for example Org. Reactions 11 (1960), 189-260 and J. Org. Chem.42 (1977), 2431}:

The diazonium salt can be obtained advantageously in a manner known perse by reacting a 3-pyrazolylaniline VIII with a nitrite such as sodiumnitrite and potassium nitrite in an aqeous solution of an acid, eg. inhydrochloric acid, hydrobromic acid or sulfuric acid.

However, it is also possible to carry out the process under anhydrousconditions, eg. in hydrogen chloride-containing glacial acetic acid, inabsolute alcohol, in dioxane or tetrahydrofuran, in acetonitrile or inacetone, in which case the aniline VIII is reacted with a nitrose ester,such as tert-butyl nitrite and isopentyl nitrite.

The subsequent Meerwein reaction of the diazonium salt with an olefin oralkyne in the presence of a copper salt, preferably a copper halide suchas copper(I) chloride, copper(II) chloride, copper(I) bromide andcopper(II) bromide, can be carried out, for example, in water, in aketone such as acetone, diethyl ketone and methyl ethyl ketone, in anitrile such as acetonitrile, in an ether such as dioxane andtetrahydrofuran or in an alcohol such as methanol and ethanol.

Diazotization and arylation can be carried out at from (−30) to +50° C.The reactants in the diazotization reaction are normally employed in anapproximately stoichiometric ratio, but an excess of one or the otherreactant may be advantageous.

In general, the olefins to be arylated are employed in a large excess;however, it is also possible to employ only a small excess or astoichiometric or substoichiometric amount.

The copper halide is normally employed in an approximatelystoichiometric amount based on the diazonium salt or, if the latter hasnot been isolated, based on the aniline VIII, but an excess orsubstoichiometric amount is also possible.

Diazotization and arylation can also be carried out in one step. In thiscase, the diazotization is effected in the presence of the olefin oralkyne component and of the copper halide.

D) Basic elimination of hydrogen halide from 3-phenylpyrazoles offormula I in which X represents —CH₂—CH(halogen)— or —CH═C(halogen)—:

Examples of bases which are suitable for this purpose are amines such astriethylamine and pyridine, alkali metal hydroxides such as sodiumhydroxide, alkali metal carbonates such as sodium carbonate andpotassium carbonate, or alkali metal hydrides such as sodium hydride.

Examples of suitable solvents are aliphatic or aromatic hydrocarbonssuch as n-hexane and toluene, halogenated hydrocarbons such asdichloromethane, ethers such as diethyl ether and tetrahydrofuran,aprotic solvents such as dimethylformamide and acetonitrile, andmixtures of these.

If appropriate, the reaction can proceed simultaneously with otherbase-catalyzed reactions—as described above under A) to C)—, for examplewhen I is formed from III (process A), when III is formed from II viathe acid chloride route (process A), when I is formed from V (process B)or else when I is formed from VIII (process C).

Those 3-pyrazolylphenylcarboxylic acids II, 3-pyrazolylbenzaldehydes Vand 3-pyrazolylanilines VIII which are mentioned as precursors inprocesses A) to C) are generally known or can be obtained by methodssimilar to known processes. Those starting materials II, V and VIIIwhere R³ is fluorine are accessible, for example, by fluorinating thecorresponding compounds where R³=hydrogen:

R^(b) is hydrogen, halogen or a group which is inert to fluorination,such as C₁-C₄-alkyl and (C₁-C₄-alkoxy)carbonyl.

Examples of suitable fluorinating reagents are fluorine, sulfurtetrafluoride, N-fluoro-2-pyridone, N-fluoropyridinium fluoride,N-fluoro-N-methyltoluenesulfonamide, nitrogen trifluoride, SELECTFLUOR®{1-chloromethyl-4-fluoro-1,4-diazabicyclo[2.2.2]octainebis(tetrafluoroborate)}, N-fluoro-benzenesulfonimide,1-fluoroquinuclidinium triflate, acetyl hypofluorite or otherconventionally used fluorinating agents {see, for example, D. T. Meshri,ACS Monogr. 187 (1995), 25}.

Particularly suitable as solvents are aliphatic or aromatic hydrocarbonswhich may be partially or fully fluorinated or chlorinated, such asn-hexane, toluene, dichloromethane and fluorotrichloromethane, etherssuch as diethyl ether and tetrahydrofuran, nitriles such asacetonitrile, and mixtures of these.

The process products of the formula X can subsequently be converted intothe compounds of the formula II, V or VIII (where in each caseR³=fluorine) by processes known per se as they are described, forexample, in WO 97/02251.

Unless otherwise specified, all the above-described processes areexpediently carried out under atmospheric pressure or under the inherentpressure of the reaction mixture in question.

The substituted 3-phenylpyrazoles I can normally be prepared by one ofthe synthesis methods mentioned above. However, for reasons of economyor process engineering, it may be more expedient to prepare somecompounds I from similar 3-phenylpyrazoles which, however, differ inparticular with regard to the meaning of the radical R⁶ or R⁷, thepreparation being carried out in a manner known per se, eg. byalkylation, acetal hydrolysis, acetalization, amidation, esterhydroysis, condensation reaction, oxidation, Peterson olefination,reduction, etherification, electrification or Wittig reaction.

Those starting compounds for the individual processes which are notalready known can be obtained in a manner known per se or by a methodsimilar to one of the processes described.

The reaction mixtures are generally worked up by methods known per se,for example

by diluting the reaction solution with water followed by isolation ofthe product by means of filtration, crystallization or solventextraction, or

removing the solvent, partitioning the residue in a mixture of water anda suitable organic solvent and working up the organic phase to give theproduct.

The substituted 3-phenylpyrazoles I may be obtained from the preparationin the form of isomer mixtures, but, if desired, the latter can beseparated into the essentially pure isomers by the methodsconventionally used for this purpose, such as crystallization orchromatography, also on an optically active adsorbate. Pure opticallyactive isomers may be prepared advantageously from correspondingoptically active starting materials.

Agriculturally useful salts of the compounds I can be formed by reactingthem with a base of the corresponding cation, preferably an alkali metalhydroxide or alkali metal hydride, or by reacting them with an acid ofthe corresponding anion, preferably of hydrochloric acid, hydrobromicacid, sulfuric acid, phosphoric acid or nitric acid.

Salts of I whose metal ion is not an alkali metal ion can also beprepared by double decomposition of the corresponding alkali metal saltin the customary manner, and ammonium, phosphonium, sulfonium andsulfoxonium salts by means of ammonia, phosphonium hydroxide, sulfoniumhydroxide, or sulfoxonium hydroxide.

The compounds I and their agriculturally useful salts, as isomermixtures and also in the form of the pure isomers, are suitable asherbicides. The herbicidal compositions comprising I effect very goodcontrol of vegetation on non-crop areas, especially at high rates ofapplication. In crops such as wheat, rice, maize, soybeans and cotton,they act against broad-leaved weeds and grass weeds without damaging thecrop plants substantially. This effect is observed especially at lowrates of application.

Depending on the application method in question, the compounds I, or theherbicidal compositions comprising them, can additionally be employed ina further number of crop plants for eliminating undesirable plants.Suitable crops are, for example, the following:

Allium cepa, Ananas comosus, Arachis hypogaea, Asparagus officinalis,Beta vulgaris spec. altissima, Beta vulgaris spec. rapa, Brassica npausvar. napus, Brassica napus var. napobrassica, Brassica rapa var.silvestris, Camellia sinensis, Carthamus tinctorius, Caryaillionoiensis, Citrus limon, Citrus sinensis, Coffea arabica (Coffeacanephora, Coffea liberica), Cucumis sativus, Cynodon dactylon, Daucuscarota, Elaeis guineensis, Fragaria vesca, Glycine max, Gossypiumhirsutum, (Gossypium arboreum, Gossypium herbaceum, Gossypiumvitifolium), Helianthus annuus, Hevea brasiliensis, Hordeum vulgare,Humulus lupulus, Iopmoea batatas, Juglans regia, Lens culinaris, Linumusitatissiumum, Lycopersicon lycopersicum, Malus spec., Manihotesculenta, Medicago sativa, Musa spec., Nicotiana tabacum (N. rustica),Olea europaea, Oryza sativa, Phaseolus lunatus, Phaseolus vulgaris,Picea abies, Pinus spec., Pisum sativum, Prunus avium, Prunus persica,Pyrus communis, Ribes sylvestre, Ricinus communis, Saccharumofficinarum, Secale cereale, Solanum tuberosum, Sorghum bicolor (S.vulgare), Theobroma cacao, Trifolium pratense, Triticum aestivum,Triticum durum, Vicia faba, Vitis vinifera and Zea mays.

In addition, the compounds I can also be used in crops which toleratethe action of herbicides due to breeding, including genetic engineeringmethods.

The compounds I, or the herbicidal compositions comprising them, can beapplied, for example, in the form of directly sprayable aqueoussolutions, powders, suspensions, also highly-concentrated aqueous, oilyor other suspensions or dispersion, emulsions, oil dispersions, pastes,dusts, materials for spreading or granules, by means of spraying,atomizing, dusting, spreading or pouring. The use forms depend on theintended purposes; in any case, they should guarantee the finestpossible distribution of the active ingredients according to theinvention.

Suitable inert auxiliaries are essentially:

Mineral oil fractions of medium to high boiling point, such as keroseneand diesel oil, furthermore coal tar oils and oils of vegetable oranimal origin, aliphatic, cyclic and aromatic hydrocarbons, eg.paraffins, tetrahydronaphthalene, alkylated naphthalenes and theirderivatives, alkylated benzenes and their derivatives, alcohols such asmethanol, ethanol, propanol, butanol and cyclohexanol, ketones such ascyclohexanone, strongly polar solvents, eg. amines such asN-methylpyrrolidone, and water.

Aqueous use forms can be prepared from emulsion concentrates,suspensions, pastes, wettable powders or water-dispersible granules byadding water. To prepare emulsions, pastes or oil dispersions, thesubstances, as such or dissolved in an oil or solvent, can behomogenized in water by means of wetting agent, tackifier, dispersant oremulsifier. Alternatively, it is possible to prepare concentrates fromactive substance, wetting agent, tackifier, dispersant or emulsifierand, if desired, solvent or oil, and these concentrates are suitable fordilution with water.

Suitable surfactants (adjuvants) are the alkali metal salts, alkalineearth metal salts and ammonium salts of aromatic sulfonic acids, eg.ligno-, phenol-, naphthalene- and dibutylnaphthalene-sulfonic acid, andof fatty acids, of alkyl- and alkylarylsulfonates, of alkyl sulfates,lauryl ether sulfates and fatty alcohol sulfates, and the salts ofsulfated hexa-, hepta- and octadecanols and of fatty alcohol glycolethers, condensates of sulfonated naphthalene and its derivatives withformaldehyde, condensates of naphthalene or of the naphthalenesulfonicacids with phenol and formaldehyde, polyoxyethylene octylphenyl ether,ethoxylated isooctyl-, octyl- or polyglycol ether, alkylaryl polyetheralcohols, isotridecyl alcohol, fatty alcohol/ethylene oxide condensates,ethoxylated castor oil, polyoxyethylene alkyl ether or polyoxypropylenealkyl ether, lauryl alcohol polyglycol ether acetate, sorbitol esters,lignin-sulfite waste liquors or methylcellulose.

Powders, materials for spreading and dusts can be prepared by mixing orconcomitant grinding of the active substances with a solid carrier.

Granules, eg. coated granules, impregnated granules and homogenousgranules, can be prepared by binding the active ingredients to solidcarriers. Solid carriers are mineral earths such as silicas, silicagels, silicates, talc, kaolin, limestone, lime, chalk, bole, loess,clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate,magnesium oxide, ground synthetic materials, fertilizers such asammonium sulfate, ammonium phosphate, ammonium nitrate, ureas, andproducts of vegetable origin such as cereal meal, tree bark meal, woodmeal and nutshell meal, cellulose powders, or other solid carriers.

The concentrations of the active ingredients I in the ready-to-useproducts can be varied within wide ranges. In general, the formulationscomprise approximately from 0.001 to 98% by weight, preferably 0.01 to95% by weight, of at least one active ingredient. The active ingredientsare employed in a purity of from 90% to 100%, preferably 95% to 100%(according to NMR spectrum).

The formulation examples which follow illustrate the preparation of suchproducts:

I. 20 parts by weight of the compound No. Ia.2 are dissolved in amixture composed of 80 parts by weight of alkylated benzene, 10 parts byweight of the adduct of 8 to 10 mol of ethylene oxide to 1 mol of oleicacid N-monoethanolamide, 5 parts by weight of calciumdodecylbenzenesulfonate and 5 parts by weight of the adduct of 40 mol ofethylene oxide and 1 mol of castor oil. Pouring the solution into100,000 parts by weight of water and finely distributing it thereingives an aqueous dispersion which comprises 0.02% by weight of theactive ingredient.

II. 20 parts by weight of the compound No. Ia.689 are dissolved in amixture composed of 40 parts by weight of cyclohexanone, 30 parts byweight of isobutanol, 20 parts by weight of the adduct of 7 mol ofethylene oxide to 1 mol of isooctylphenol and 10 parts by weight of theadduct of 40 mol of ethylene oxide to 1 mol of castor oil. Pouring thesolution into 100,000 parts by weight of water and finely distributingit therein gives an aqueous dispersion which comprises 0.02% by weightof the active ingredient.

III. 20 parts by weight of the active ingredient No. Ia.1322 aredissolved in a mixture composed of 25 parts by weight of cyclohexanone,65 parts by weight of a mineral oil fraction of boiling point 210° to280° C. and 10 parts by weight of the adduct of 40 mol of ethylene oxideand 1 mol of castor oil. Pouring the solution into 100,000 parts byweight of water and finely distributing it therein gives an aqueousdispersion which comprises 0.02% by weight of the active ingredient.

IV. 20 parts by weight of the active ingredient No. Ia.1331 are mixedthoroughly with 3 parts by weight of sodiumdiisobutylnaphthalene-α-sulfonate, 17 parts by weight of the sodium saltof a lignosulfonic acid from a sulfite waste liquor and 60 parts byweight of pulverulent silica gel, and the mixture is ground in a hammermill. Finely distributing the mixture in 20,000 parts by weight of watergives a spray mixture which comprises 0.1% by weight of the activeingredient.

V. 3 parts by weight of the active ingredient No. Ig.1310 are mixed with97 parts by weight of finely divided kaolin. This gives a dust whichcomprises 3% by weight of the active ingredient.

VI. 20 parts by weight of the active ingredient No. Ia.1334 are mixedintimately with 2 parts by weight of calcium dodecylbenzenesulfonate, 8parts by weight of fatty alcohol polyglycol ether, 2 parts by weight ofthe sodium salt of a phenol/urea/formaldehyde condensate and 68 parts byweight of a paraffinic mineral oil. This gives a stable oil dispersion.

VIII. 1 part by weight of the active ingredient No. Ia.2270 is dissolvedin a mixture composed of 70 parts by weight of cyclohexanone, 20 partsby weight of ethoxylated isooctylphenol and 10 parts by weight ofethoxylated castor oil. This gives a stable emulsion concentrate.

VIII. 1 part by weight of the active ingredient No. Ik.1310 is dissolvedin a mixture composed of 80 parts by weight of cyclohexanone and 20parts by weight of Wettol® EM 31 (=non-ionic emulsifier based onethoxylated castor oil; BASF AG). This gives a stable emulsionsconcentrate.

The active ingredients I, or the herbicidal compositions, can be appliedpre- or post-emergence. If the active ingredients are less welltolerated by certain crop plants, it is possible to use applicationtechniques in which the herbicidal compositions are sprayed, with theaid of the spraying equipment, in such a way that they come into aslittle contact as possible, if any, with the leaves of the sensitivecrop plants while reaching the leaves of undersirable plants which growunderneath, or the bare soil surface (post-directed, lay-by).

Depending on the intended aim, the season, the target plant and thegrowth stage, the rates of application of active ingredient I are from0.001 to 3.0, preferably 0.01 to 1.0, kg of active substance (a.s.)/ha.

To widen the spectrum of action and to achieve synergistic effects, thesubstituted 3-phenylpyrazoles I may be mixed, and applied jointly, witha large number of representatives of other groups of herbicidally orgrowth-regulating active ingredients. Suitable examples of components inmixtures are 1,2,4-thiadiazoles, 1,3,4-thiadiazoles, amides,aminophosphoric acid and its derivatives, aminotriazoles, anilides,aryloxy/hetaryloxyalkanoic acids and their derivatives, benzoic acid andits derivatives, benzothiadiazinones,2-(hetaroyl/aroyl)-1,3-cyclohexanediones, hetaryl aryl ketones,benzylisoxazolidinones, meta-CF₃-phenyl derivatives, carbamates,quinolinecarboxylic acid and its derivatives, chloroacetanilides,cyclohexane-1,3-dione derivatives, diazines, dichloropropionic acid andits derivatives, dihydrobenzofurans, dihydrofuran-3-ones,dinitroanilines, dinitrophenols, diphenyl ethers, dipyridyls,halocarboxylic acids and their derivatives, ureas, 3-phenyluracils,imidazoles, imidazolinones, N-phenyl-3,4,5,6-tetrahydrophthalimides,oxadiazoles, oxiranes, phenoles, aryloxy- and hetaryloxyphenoxypropionicesters, phenylacetic acid and its derivatives, 2-phenylpropionic acidand its derivatives, pyrazoles, phenylpyrazoles, pyridazines,pyridinecarboxylic acid and its derivatives, pyrimidyl ethers,sulfonamides, sulfonylureas, triazines, triazinones, triazolinones,triazolecarboxamides and uracils.

Moreover, it may be advantageous to apply the compounds I, alone or incombination with other herbicides, in the form of a mixture with evenfurther crop protection agents, for example with pesticides or agentsfor controlling phytopathogenic fungi or bacteria. Also of interest isthe miscibility with mineral salt solutions which are employed fortreating nutritional and trace element deficiencies. Non-phytotoxic oilsand oil concentrates may also be added.

PREPARATION EXAMPLES Example 1

MethylN-methoxy-2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorobenzimidate(No. Ia.2)

A solution of 1 g (2.6 mmol) ofN-methoxy-2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorobenzamidein 50 ml of acetone was treated with 0.43 g (3.1 mmol) of potassiumcarbonate and 0.39 g (3.1 mmol) of dimethyl sulfate. After 3 days, themixture was concentrated. The residue was treated with water, whereuponthe mixture was extracted twice using ethyl acetate. The combinedorganic phases were washed with water and saturated aqueous sodiumchloride solution, dried over magnesium sulfate and finallyconcentrated. The crude product was purified by means of columnchromatography on silica gel (eluent:hexane/ethyl acetate=2:1). Yield:0.2 g.

¹H NMR (270 MHz, in CDCl₃): δ [ppm]=3.73 (s,3H), 3.85 (s,3H), 3.90(s,3H), 6.71 (t,1H), 7.32 (d,1H), 7.68 (d,1H).

Precursor 1.1

2-Chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorobenzoylchloride

A solution of 8 g (22 mmol) of2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorobenzoicacid in 100 ml of toluene was treated with 1 drop of dimethylformamideand 8.6 g (67 mmol) of oxalyl chloride. After the mixture had beenstirred for 30 minutes at reflux temperature, it was cooled andconcentrated. Yield: quantitative.

Precursor 1.2

N-Methoxy-2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorobenzamide

A solution of 8.4 g (22 mmol) of2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorobenzoylchloride in 150 ml of toluene was treated with 34 g (0.24 mol) ofpotassium carbonate, and 16 g (48 mmol) of a 25% strength aqueousmethoxyamine hydrochloride solution was subsequently added dropwise.After the reaction mixture had been stirred for 4 hours, it was dilutedwith 0.5 l of water. The organic phase was then separated off, washedwith saturated aqueous sodium chloride solution, dried over magnesiumsulfate and finally concentrated. Yield: 8.3 g.

¹H NMR (270 MHz, in CDCl₃): δ [ppm]=3.83 (s,3H), 3.90 (s,3H), 6.71(t,1H), 7.25 (d,1H), 7.79 (d,1H), 9.20 (s,1H).

Example 2

N-Methoxy-2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorobenzimidicacetic anhydride (No. Ia.686)

0.26 g (2.6 mmol) of triethylamine and 0.23 g (2.9 mmol) of acetylchloride were added dropwise in succession to a solution of 1 g (2.6mmol) ofN-2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluoro(methoxy)benzamidein 46 ml of dichloromethane. After the reaction mixture had been stirredfor 16 hours, it was treated with water. The organic phase wassubsequently separated off, dried over magnesium sulfate and finallyconcentrated. The crude product was purified by means of silica gelchromatography (eluent:hexane/ethyl acetate=1:2). Yield: 0.3 g.

Example 3

AllylN-methoxy-2-chloro-5-(4-chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yl)-4-fluorobenzimidate(No. Ic.590)

A solution of 1.5 g (3.9 mmol) ofN-methoxy-2-chloro-5-(4-chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yl)-4-fluorobenzamidein 50 ml of acetone was treated with 0.6 g (4.6 mmol) of potassiumcarbonate and 0.6 g (4.6 mmol) of allyl bromide. After the mixture hadbeen stirred for 16 hours, it was concentrated. The residue was treatedwith water. The product of value was subsequently extracted twice usingethyl acetate. The combined organic phases were washed with water andsaturated aqueous sodium chloride solution, dried over magnesium sulfateand finally concentrated. The crude product was purified by columnchromatography on silica gel (eluent:hexane/ethyl acetate=2:1). Yield:0.3 g.

Precursor 3.1

2-Chloro-5-(4-chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yl)-4-fluorobenzoylchloride

14 g (39 mmol) of2-chloro-5-(4-chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yl)-4-fluorobenzoicacid were reacted by a method similar to the one given for precursor1.1. Yield: 13.3 g.

Precursor 3.2

N-Methoxy-2-chloro-5-(4-chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yl)-4-fluorobenzamide

13.7 g (36 mmol) of2-chloro-5-(4-chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yl)-4-fluorobenzoylchloride were reacted by a method similar to the one described forprecursor 1.2. Yield: 14 g.

¹H NMR (270 MHz, in CDCl₃): δ [ppm]=3.90 (s,3H), 4.06 (s,3H), 7.27(d,1H), 7.79 (d,1H), 9.05 (s,1H).

Example 4

MethylN-methoxy-2-chloro-3-(2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorophenyl)acrylimidate(No. Ig.2)

A solution of 1 g ofN-Methoxy-2-chloro-3-(2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorophenyl)acrylamide(2.3 mmol) in 30 ml of acetone was treated with 0.4 g (2.7 mmol) ofpulverulent potassium carbonate and 0.35 g (2.5 mmol) of methyl iodide.After the mixture had been stirred for 16 hours, it was concentrated.The residue was treated with water and ethyl acetate. The organic phasewas dried over magnesium sulfate and then concentrated. The residue waspurified by means of column chromatography on silica gel(eluent:hexane/ethyl acetate=4:1). Yield: 0.2 g.

Precursor 4.1

tert-Butyl2-chloro-3-(2-chloro-5-(4-chloro-5-dilfuoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorophenyl)acrylate

A solution of 32 g of2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorobenzaldehyde(94 mmol) in 200 ml of toluene was treated with 72 g (0.14 mol) oftertbutoxycarbonyl(chloro)methylene(triphenyl)phosphorane. After themixture had been stirred for 16 hours, it was concentrated. The residuewas treated with ethyl acetate. The mixture was then heated at refluxtemperature and filtered while hot. The solids removed were washedrepeatedly with ethyl acetate. The filtrate was treated withapproximately twice the volume of hexane, whereupon the mixture wasrefiltered. Finally, the filtrate was concentrated. The crude productwhich remained was purified from residual triphenylphosphine oxide bydissolving it in hexane/ethyl acetate (4:1) followed by filtrationthrough a silica gel bed. Yield: 44 g.

¹H NMR (250 MHz, in CDCl₃): δ [ppm]=1.58 (s,9H), 3.84 (s,3H), 6.73(t,1H), 7.32 (d,1H), 8.03 (s,1H), 8.24 (d,1H).

Precursor 4.2

2-Chloro-3-(2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorophenyl)acrylicacid

A solution of 44 g of tert-butyl2-chloro-3-(2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorophenyl)acrylate(93 mmol) in 200 ml of dichloromethane was treated with 200 ml oftrifluoroacetic acid. After the mixture had been stirred for 16 hours,it was concentrated. The residue was recrystallized from hexane/ethylacetate (2:1). Yield: 23 g; a further 4 g by concentrating the motherliquor.

¹H NMR (270 MHz, in CDCl₃): δ [ppm]=3.87 (s,3H), 6.72 (t,1H), 7.34(d,1H), 8.26 (s,1H), 8.31 (d,1H).

Precursor 4.3

2-Chloro-3-(2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorophenyl)acryloylchloride

A solution of 27 g of2-chloro-3-(2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorophenyl)acrylicacid (64 mmol) in 200 ml of toluene was treated with 3 drops ofdimethylformamide and 33 g (0.26 mol) of oxalyl chloride. The mixturewas subsequently stirred at 90° C. until the vigorous evolution of gashad ceased (after approximately 2.5 hours). The reaction mixture wasthen concentrated. Yield: 26 g of crude product which was furtherreacted without purification.

Precursor 4.4

N-Methoxy-2-chloro-3-(2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorophenyl)acrylamide

A solution of 4.5 g (10 mmol) of2-chloro-3-(2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorophenyl)acryloylchloride in 25 ml of toluene was treated with 25 ml of water, 14.4 g(0.1 mol) of potassium carbonate and 1.7 g (20 mmol) of methoxyaminehydrochloride. After the mixture had been stirred for 16 hours atapproximately 20° C., it was heated for a further 2 hours at 40° C. Thereaction mixture was subsequently diluted with 200 ml of toluene and 200ml of water. The solids were then filtered off. The organic phase wasdried over magnesium sulfate and finally concentrated. Yield: 3.1 g.

¹H NMR (270 MHz, in CDCl₃): δ [ppm]=3.85 (s,3H), 3.90 (s,3H), 6.73(t,1H), 7.33 (d,1H), 8.04 (d,1H), 8.20 (s,1H), 9.33 (s,1H).

Example 5 MethoxycarbonylmethylN-methoxy-2-chloro-3-[2-chloro-5-(4-chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yl)-4-fluorophenyl]acrylimide(No. Ik.1310)

A solution of 1.2 g (2.6 mmol) ofN-methoxy-2-chloro-3-(2-chloro-5-(4-chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yl)-4-fluorophenyl)acrylamidein 50 ml of acetone was treated with 0.4 g (3 mmol) of potassiumcarbonate and 0.4 g (2.9 mmol) of methyl bromoacetate. After the mixturehad been stirred for 16 hours, it was concentrated. The residue wastreated with water. The product was then extracted with diethyl ether.The organic phase was dried over magnesium sulfate and subsequentlyconcentrated. The crude product is purified by means of silica gelchromatography (eluent:hexane/ethyl acetate=4:1). Yield: 0.6 g.

Precursor 5.1

tert-Butyl2-chloro-3-[2-chloro-5-(4-chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yl)-4-fluorophenyl]acrylate

6 g (18 mmol) of2-chloro-5-(4-chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yl)-4-fluorobenzaldehydewere reacted by a method similar to the one described for precursor 4.1.Yield: 6.4 g.

¹H NMR (270 MHz, in CDCl₃): δ [ppm]=1.58 (s,9H), 4.07 (s,3H), 7.33(d,1H), 8.03 (s,1H), 8.20 (d,1H).

Precursor 5.2

2-Chloro-3-[2-chloro-5-(4-chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yl)-4-fluorophenyl]acrylicacid

4.8 g (10 mmol) of2-chloro-3-[2-chloro-5-(4-chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yl)-4-fluorophenyl]acrylicacid were treated by a method similar to the one described for precursor4.2. Yield: 2.4 g. M.p.: 195-196° C.

Precursor 5.3

2-Chloro-3-[2-chloro-5-(4-chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yl)-4-fluorophenyl]acryloylchloride

1.7 g (4 mmol) of2-chloro-3-[2-chloro-5-(4-chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yl)-4-fluorophenyl]acrylicacid were reacted by a method similar to the one described for precursor4.3. Yield: 1.7 g.

Precursor 5.4

N-Methoxy-2-chloro-3-[2-chloro-5-(4-chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yl)-4-fluorophenyl]acrylamide

1.7 g (3.9 mmol) of2-chloro-3-[2-chloro-5-(4-chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yl)-4-fluorophenyl]acryloylchloride were reacted by a method similar to the one described forprecursor 4.4. Yield: 1.2 g.

¹H NMR (270 MHz, in CDCl₃): δ [ppm]=3.90 (s,3H), 4.08 (s,3H), 7.34(d,1H), 8.00 (d,1H), 8.21 (s,1H), 9.36 (s,1H).

Example 6

MethylN-methoxy-2-chloro-5-(4-chloro-1-methyl-5-methylsulfonyl-1H-pyrazol-3-yl)-4-fluorobenzamidate(No. Ie.2)

Using 1.4 g (3.5 mmol) ofN-methoxy-2-chloro-5-(4-chloro-1-methyl-5-methylsulfonyl-1H-pyrazol-3-yl)-4-fluorobenzamide,0.58 g (4.2 mmol) of potassium carbonate and 0.53 g (4.2 mmol) ofdimethyl sulfate and following the procedure described in Example 1, 0.2g of the product of value was obtained.

Precursor 6.1

2-Chloro-5-(4-chloro-5-(4-chloro-1-methyl-5-methylsulfonyl-1H-pyrazol-3-yl)-4-fluorobenzoicacid were reacted in a manner similar to precursor 1.1. Yield:quantitative.

Precursor 6.2

N-methoxy-2-chloro-5-(4-chloro-1-methyl-5-methylsulfonyl-1H-pyrazol-3-yl)-4-fluorobenzamide

5 g (13 mmol) of2-chloro-5-(4-chloro-1-methyl-5-methylsulfonyl-1H-pyrazol-3-yl)-4-fluorobenzoylchloride were reacted in a manner similar to precursor 1.2. Yield: 2.8g.

¹H NMR (250 MHz, in CDCl₃): δ [ppm]=3.30 (s,3H), 3.91 (s,3H), 4.15(s,3H), 7.29 (d,1H), 7.82 (d,1H), 8.95 (s,1H).

Example 7

2-Methoxyimino)ethylN-methoxy-3-[2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorophenyl]propiolimide(No. Ip.1094)

0.4 g (2.7 mmol) of potassium carbonate and 0.27 g (2.5 mmol) ofO-methyl chloroacetaldehyde oxime were added to a solution of 1 g (2.3mmol) ofN-methoxy-2-chloro-3-[2-chloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-4-fluorophenyl]acrylamidein 50 ml of acetone. After the mixture had been stirred for 3 days, itwas concentrated. The residue was treated with 50 ml ofdimethylformamide. The mixture was subsequently heated for 4 more hoursat 100° C. and then reconcentrated. Then, the residue was treated with20 ml of ethyl acetate. The resulting organic phase was washed withwater, dried over magnesium sulfate and finally concentrated. The crudeproduct was purified by means of silica gel chromatography(eluent:hexane/ethyl acetate=2:1). Yield: 0.2 g.

Example 8 MethylN-methoxy-2,4-dichloro-5-(5-difluoromethoxy-4-fluoro-1-methyl-1H-pyrazol-3-yl)benzimidate(No. Ib.3)

Using 0.5 g (1.3 mmol) ofN-methoxy-2,4-dichloro-5-(5-difluoromethoxy-4-fluoro-1-methyl-1H-pyrazol-3-yl)benzamide,0.21 g (1.6 mmol) of potassium carbonate and 0.20 g (1.6 mmol) ofdimethyl sulfate and following the procedure described in Example 1,0.17 g of the desired produce of value was obtained.

Precursor 8.1

3-(2,4-Dichloro-5-methylphenyl)-5-difluoromethoxy-4-fluoro-1-methyl-1H-pyrazole

46.3 g (131 mmol) of Selectfluor™ were added to a solution of 40.2 g(131 mmol) of3-(2,4-dichloro-5-methylphenyl)-5-difluoromethoxy-1-methyl-1H-pyrazolein 0.5 l of acetonitrile. After the mixture had been stirred for 12hours at room temperature, it was heated for a further hour at refluxtemperature. Thereafter, three batches of 6.9 g (20 mmol) ofSelectfluor™ were added to the reaction mixture, a little at a time, andthe mixture was heated in each case for one hour at reflux temperature.The resulting mixture was subsequently treated with 0.5 l of methyltert-butyl ether. The organic phase was washed with water, saturatedaqueous sodium hydrogen carbonate solution and again with water, thendried over magnesium sulfate and finally concentrated. The crude productwas purified by means of silica gel chromatography (eluent:hexane/ethylacetate=9:1). Yield: 20.3 g.

¹H NMR (400 MHz, in CDCl₃): δ [ppm]=2.36 (s,3H), 3.78 (s,3H), 6.66(t,1H), 7.37 (s,1H), 7.46 (s,1H).

Precursor 8.2

2,4-Dichloro-5-(5-difluoromethoxy-4-fluoro-1-methyl-1H-pyrazol-3-yl)benzaldehyde

A solution of 20.3 g (62 mmol) of3-(2,4-dichloro-5-methylphenyl)-5-difluoromethoxy-4-fluoro-1-methyl-1H-pyrazoleand 11.1 g (62 mmol) of N-bromosuccinimide in 0.27 l oftetrachloromethane was heated for two hours at reflux temperature whileexposed to a UV lamp. Then, two portions of 2.2 g (12 mmol) ofN-bromosuccinimide were added to the reaction mixture, a little at atime, whereupon in each case the mixture was heated to refluxtemperature while being exposed again. The mixture was then allowed tocool, and the solids were filtered off. The filtrate was concentrated.

14.2 g (120 mmol) of N-methylmorpholin-N-oxide were subsequently addedto the above substance, dissolved in 500 ml of acetonitrile. The mixturewas stirred for 3 hours and then concentrated. The residue was treatedwith 500 ml of water and 500 ml of dichloromethane. To isolate theproduct, the organic phase was separated off, washed three times withwater, then dried over magnesium sulfate and finally concentrated. Theresidue was purified by means of MPLC on silica gel(eluent:cyclohexane/ethyl acetate=9.1). Yield: 7.4 g.

¹H NMR (270 MHz, in CDCl₃): δ [ppm]=3.8 (s,3H), 6.67 (t,1H), 7.63(s,1H), 8.09 (s,1H), 10.43 (s,1H).

Precursor 8.3

2,4-Dichloro-5-(5-difluoromethoxy-4-fluoro-1-methyl-1H-pyrazol-3-yl)benzoicacid

First, a solution of 0.85 g (5.5 mmol) of sodium dihydrogen phosphatedihydrate in 10 ml of water and then 2.7 ml of a 30% strength aqueoushydrogen peroxide solution were added dropwise to a solution of 7.4 g(22 mmol) of2,4-dichloro-5-(5-difluoromethoxy-4-fluoro-1-methyl-1H-pyrazol-3-yl)benzaldehydein 200 ml of acetonitrile. A solution of 2.9 g (33 mmol) of sodiumchloride in 25 ml of water was then added dropwise to the reactionmixture in the course of 20 minutes. After the solution had been stirredfor one hour, the resulting mixture was acidified with dilutehydrochloric acid. Finally, the solid product of value which had formedwas filtered off and dried. Yield: 6.3 g.

¹H NMR (250 MHz, in CDCl₃): δ [ppm]=3.83 (s,3H), 6.67 (t,1H), 7.64(s,1H), 8.21 (s,1H).

Precursor 8.4

2,4-Dichloro-5-(5-fluoromethoxy-4-fluoro-1-methyl-1H-pyrazol-3-yl)benzoylchloride

5.8 g (16 mmol) of2,4-dichloro-5-(5-difluoromethoxy-4-fluoro-1-methyl-1H-pyrazol-3-yl)benzoicacid and 10.4 g (82 mmol) of oxalyl chloride were reacted in the mannerdescribed for Precursor 1.1. Yield: 5.2 g.

Precursor 8.5

N-methoxy-2,4-dichloro-5-(5-difluoromethoxy-4-fluoro-1-methyl-1H-pyrazol-3-yl)benzamide

Using 5.2 g (14 mmol) of2,4-dichloro-5-(5-difluoromethoxy-4-fluoro-1-methyl-1H-pyrazol-3-yl)benzoylchloride, 19.2 g (0.14 mol) of potassium carbonate and 9.2 g (28 mmol)of a 25% strength aqueous methoxyamine hydrochloride solution andfollowing the procedure described for Precursor 1.2, a crude product wasobtained whose purification by means of silica gel chromatography(eluent:hexane/ethyl acetate=4:1) gave 1.5 g of the desired product ofvalue.

¹H NMR (250 MHz, in CDCl₃): δ [ppm]=3.79 (s,3H), 3.90 (s,3H), 6.66(t,1H), 7.55 (s,1H), 7.74 (s,1H), 9.00 (s,1H).

In addition to above-described active ingredients, Table 2 below listsfurther substituted 3-phenylpyrazoles I which were, or can be, preparedby a method similar to the one described above:

TABLE 2 I

No. R² R³ R⁴ R⁶ R⁷ X M.p./¹H NMR [ppm]/MS [m/z] Ia.2 OCHF₂ Cl F CH₃ CH₃Bond 107-108° C. Ia.3 OCHF₂ Cl Cl CH₃ CH₃ Bond 3.74(s, 3H), 3.85(s, 3H),3.90(s, 3H), 6.71(t, 1H), 7.53(s, 1H), 7.62(s, 1H) Ia.5 OCHF₂ Cl F C₂H₅CH₃ Bond 1.34(t, 3H), 3.84(s, 3H), 3.90(s, 3H), 3.96(q, 2H), 6.70(t,1H), 7.30(d, 1H), 7.68(d, 1H) Ia.32 OCHF₂ Cl F CH₃ C₂H₅ Bond 96-97° C.Ia.35 OCHF₂ Cl F C₂H₅ C₂H₅ Bond 87-88° C. Ia.446 OCHF₂ Cl F CH₂—CH₂—OCH₃CH₃ Bond 3.35(s, 3H), 3.65(t, 2H), 3.84(s, 3H), 3.89(s, 3H), 4.11(t,2H), 6.72(t, 1H), 7.29(d, 1H), 7.72(d, 1H) Ia.461 OCHF₂ Cl FCH₂—CH₂—OCH₃ CH₂—C≡CH Bond 2.47(s, 1H), 3.38(s, 3H), 3.64(t, 2H),3.83(s, 3H), 4.65(s, 2H), 4.13(t, 2H), 4.68(d, 2H), 6.69(t, 1H), 7.29(d,1H), 7.72(d, 1H) Ia.590 OCHF₂ Cl F CH₂—CH═CH₂ CH₃ Bond 54-56° C. Ia.593OCHF₂ Cl F CH₂—CH═CH₂ C₂H₅ Bond 1.32(t, 3H), 3.85(s, 3H), 4.15(q, 2H),4.49(d, 2H), 5.12(d, 1H), 5.29(d, 1H), 5.92(m, 1H), 6.72(t, 1H), 7.30(d,1H), 7.68(d, 1H) Ia.602 OCHF₂ Cl F CH₂—CH═CH₂ CH₂—CH═CH₂ Bond 75-77° C.Ia.686 OCHF₂ Cl F CO—CH₃ CH₃ Bond 2.27(s, 3H), 3.85(s, 3H), 3.99(s, 3H),6.70(t, 1H), 7.28(d, 1H), 7.85(d, 1H) Ia.689 OCHF₂ Cl F CO—CH₃ C₂H₅ Bond1.32(t, 3H), 2.28(s, 3H), 3.85(s, 3H), 4.23(q, 2H), 6.72(t, 1H), 7.28(d,1H), 7.85(d, 1H) Ia.698 OCHF₂ Cl F CO—CH₃ CH₂—CH═CH₂ Bond 2.28(s, 3H),3.84(s, 3H), 4.68(d, 2H), 5.25(dd, 1H), 5.34(dd, 1H), 6.01(m, 1H),6.71(t, 1H), 7.28(d, 1H), 7.85(d, 1H) Ia.782 OCHF₂ Cl F CO—OCH₃ CH₃ Bond3.84(s, 3H), 3.89(s, 3H), 4.01(s, 3H), 6.70(t, 1H), 7.29(d, 1H), 7.85(d,1H) Ia.830 OCHF₂ Cl F CO—N(CH₃)₂ CH₃ Bond 2.93(s, 3H), 3.08(s, 3H),3.81(s, 3H), 3.97(s, 3H), 6.72(t, 1H), 7.28(d, 1H), 7.90(d, 1H) Ia.1001OCHF₂ Cl F CH₂—CO-cyclopropyl C₂H₅ Bond 0.95(m, 2H), 1.10(m, 2H),1.32(t, 3H), 2.09(m, 1H), 3.84(s, 3H), 4.15(q, 2H), 4.75(s, 2H), 6.71(t,1H), 7.29(d, 1H), 7.72(d, 1H) Ia.1094 OCHF₂ Cl F CH₂—CH═N—OCH₃ CH₃ Bond3.83(m, 6H), 3.92(m, 3H), 4.62 and 4.78(2d, together 2H), 6.73(t, 1H),6.97 and 7.49(2t, together 1H), 7.32(d, 1H), 7.71(d, 1H) Ia.1097 OCHF₂Cl F CH₂—CH═N—OCH₃ C₂H₅ Bond 1.33(t, 3H), 3.84(m, 6H), 4.14(q, 2H), 4.63and 4.80(2d, together 2H), 6.71(t, 1H), 698 and 7.50(2t, together 1H),7.30(d, 1H), 7.69(d, 1H) Ia.1214 OCHF₂ Cl F CH₂—C(═N— CH₃ Bond 3.85(s,3H), 3.87(s, 3H), 3.89(s, 3H), OCH₃)—CO—OCH₃ 4.09(s, 3H), 4.92(s, 2H),6.72(t, 1H), 7.30(d, 1H), 7.73(d, 1H) Ia.1217 OCHF₂ Cl F CH₂—C(═N— C₂H₅Bond 1.30(t, 3H), 3.85(s, 3H), 3.87(s, 3H), OCH₃)—CO—OCH₃ 4.06(s, 3H),4.12(q, 2H), 4.95(s, 2H), 6.72(t, 1H), 7.29(d, 1H), 7.72(d, 1H) Ia.1238OCHF₂ Cl F CH₂—COOH CH₃ Bond 3.74(s, 3H), 3.85(s, 3H), 4.83(s, 2H),6.70(t, 1H), 7.29(d, 1H), 7.73(d, 1H) Ia.1310 OCHF₂ Cl F CH₂—CO—OCH₃ CH₃Bond 3.74(s, 3H), 3.85(s, 3H), 3.91(s, 3H), 4.63(s, 2H), 6.70(t, 1H),7.29(d, 1H), 7.73(d, 1H) Ia.1313 OCHF₂ Cl F CH₂—CO—OCH₃ C₂H₅ Bond98-100° C. Ia.1322 OCHF₂ Cl F CH₂—CO—OCH₃ CH₂—CH═CH₂ Bond 3.72(s, 3H),3.84(s, 3H), 4.60(d, 2H), 4.68(s, 2H), 5.26(dd, 1H), 5.35(dd, 1H),6.04(m, 1H), 6.71(t, 1H), 7.29(d, 1H), 7.74(d, 1H) Ia.1325 OCHF₂ Cl FCH₂—CO—OCH₃ CH₂—C≡CH Bond 2.49(t, 1H), 3.75(s, 3H), 3.83(s, 3H), 4.65(s,2H), 4.69(d, 2H), 6.70(t, 1H), 7.29(d, 1H), 7.76(d, 1H) Ia.1331 OCHF₂ ClF CH₂—CO—OCH₃ CH₂-phenyl Bond 3.63(s, 3H), 3.81(s, 3H), 4.67(d, 2H),5.11(s, 2H), 6.69(t, 1H), 7.20-7.45(m, 6H), 7.72(d, 1H) Ia.1334 OCHF₂ ClF CH(CH₃)—CO—OCH₃ CH₃ Bond 1.61(d, 3H), 3.73(s, 3H), 3.85(s, 3H),3.88(s, 3H), 4.77(q, 1H), 6.79(t, 1H), 7.30(d, 1H), 7.73(d, 1H) Ia.1358OCHF₂ Cl F CH(C₂H₅)—CO—OCH₃ CH₃ Bond 1.08(t, 3H), 1.95(quint., 2H),3.72(s, 3H), 3.84(s, 3H), 3.89(s, 3H), 4.63(t, 1H), 6.72(t, 1H), 7.28(d,1H), 7.70(d, 1H) Ia.1382 OCHF₂ Cl F CH₂—CO—OC₂H₅ CH₃ Bond 1.28(t, 3H),3.84(s, 3H), 3.92(s, 3H), 4.19(q, 2H), 4.60(s, 2H), 6.70(t, 1H), 7.9(d,1H), 7.73(d, 1H) Ia.1454 OCHF₂ Cl F CH₂—CO—OC(CH₃)₃ CH₃ Bond 1.41(s,9H), 3.83(s, 3H), 3.92(s, 3H), 4.45(s, 2H), 6.69(t, 1H), 7.29(d, 1H),7.75(d, 1H) Ia.1694 OCHF₂ Cl F CH₂—CO—N(CH₃)₂ CH₃ Bond 468[M]⁺,424[M—N(CH₃)₂]⁺ Ia.1877 OCHF₂ Cl F CH₂-phenyl CH₂—C≡CH Bond 2.48(t, 1H),3.81(s, 3H), 4.68(d, 2H), 5.03(s, 2H), 6.69(t, 1H), 7.20-7.35(m, 6H),7.52(d, 1H) Ia.1883 OCHF₂ Cl F CH₂-phenyl CH₂-phenyl Bond 3.82(s, 3H),5.05(s, 2H), 5.14(s, 2H), 6.69(t, 1H), 7.20-7.50(m, 12H) Ia.2270 OCHF₂Cl F CH₃ CH₂—CH═CH₂ Bond 88-89° C. Ia.2330 OCHF₂ Cl F CH₃ CH₂—C≡CH Bond2.49(t, 1H), 3.74(s, 3H), 3.84(s, 3H), 4.68(d, 2H), 6.71(t, 1H), 7.32(d,1H), 7.68(d, 1H) Ia.2534 OCHF₂ Cl F CH₃ CH₂—CO—OCH₃ Bond 455[M]⁺ Ia.2666OCHF₂ Cl F CH₃ CH₂—CO—OC(CH₃)₃ Bond 1.48(s, 9H), 3.78(s, 3H), 3.84(s,3H), 4.51(s, 2H), 6.70(t, 1H), 7.31(d, 1H), 7.68(d, 1H) Ia.2954 OCHF₂ ClF CH₃ CH₂-phenyl Bond 3.74(s, 3H), 3.84(s, 3H), 4.12(s, 2H), 6.70(t,1H), 7.25-7.45(m, 6H), 7.66(d, 1H) Ib.3 OCHF₂ F Cl CH₃ CH₃ Bond 3.73(s,3H), 3.79(s, 3H), 3.89(s, 3H), 6.67(t, 1H), 7.60(s, 1H), 7.63(s, 1H)Ib.1311 OCHF₂ F Cl CH₂—CO—OCH₃ CH₃ Bond 3.75(s, 3H), 3.79(s, 3H),3.91(s, 3H), 4.63(s, 2H), 6.67(t, 1H), 7.56(s, 1H), 7.67(s, 1H) Ic.2 CF₃Cl F CH₃ CH₃ Bond 3.84(s, 3H), 3.91(s, 3H), 4.08(s, 3H), 7.34(d, 1H),7.65(d, 1H) Ic.5 CF₃ Cl F C₂H₅ CH₃ Bond 1.34(t, 3H), 3.90(s, 3H),3.99(q, 2H), 4.06(s, 3H), 7.32(d, 1H), 7.64(d, 1H) Ic.590 CF₃ Cl FCH₂—CH═CH₂ CH₃ Bond 3.91(s, 3H), 4.08(s, 3H), 4.47(d, 2H), 5.23(dd, 1H),5.29(dd, 1H), 5.90(m, 1H), 7.31(d, 1H), 7.63(d, 1H) Ic.686 CF₃ Cl FCO—CH₃ CH₃ Bond 2.27(s, 3H), 3.98(s, 3H), 4.07(s, 3H), 7.29(d, 1H),3.82(d, 1H) Ic.1310 CF₃ Cl F CH₂—CO—OCH₃ CH₃ Bond 3.84(s, 3H), 3.91(s,3H), 4.07(s, 3H), 4.66(s, 2H), 7.30(d, 1H), 7.72(d, 1H) Ie.2 SO₂—CH₃ ClF CH₃ CH₃ Bond 3.32(s, 3H), 3.75(s, 3H), 390(s, 3H), 4.16(s, 2H),7.37(d, 1H), 7.68(d, 1H) Ie.662 SO₂—CH₃ Cl F CH₂—C≡CH CH₃ Bond 2.54(t,1H), 3.30(s, 3H), 3.91(s, 3H), 4.15(s, 3H), 4.71(d, 2H), 7.34(d, 1H),7.73(d, 1H) Ie.1310 SO₂—CH₃ Cl F CH₂—CO—OCH₃ CH₃ Bond 3.32(s, 3H),3.74(s, 3H), 3.92(s, 3H), 4.15(s, 3H), 4.66(s, 2H), 7.32(d, 1H), 7.73(d,1H) Ig.2 OCHF₂ Cl F CH₃ CH₃ —CH═C(Cl)— 3.85(s, 3H), 3.96(s, 3H), 4.00(s,3H), 6.72(t, 1H), 7.30(d, 1H), 7.44(s, 1H), 8.12(d, 1H) Ig.5 OCHF₂ Cl FC₂H₅ CH₃ —CH═C(Cl)— 1.42(t, 3H), 3.85(s, 3H), 3.95(s, 3H), 4.33(q, 2H),6.72(t, 1H), 7.29(d, 1H), 7.49(s, 1H), 8.11(d, 1H) Ig.590 OCHF₂ Cl FCH₂—CH═CH₂ CH₃ —CH═C(Cl)— 3.86(s, 3H), 3.97(s, 3H), 4.75(d, 2H), 5.31(d,1H), 5.40(d, 1H), 6.05(m, 1H), 6.71(t, 1H), 7.30(d, 1H), 7.51(s, 1H),8.12(d, 1H) Ig.686 OCHF₂ Cl F CO—CH₃ CH₃ —CH═C(Cl)— 2.34(s, 3H), 3.84(s,3H), 4.00(s, 3H), 6.72(t, 1H), 7.29(d, 1H), 7.37(s, 1H), 8.15(d, 1H)Ig.998 OCHF₂ Cl F CH₂—CO-cyclopropyl CH₃ —CH═C(Cl)— 1.00(m, 2H), 1.16(m,2H), 2.15(m, 1H), 3.84(s, 3H), 3.92(s, 3H), 4.98(s, 2H), 6.72(t, 1H),7.28(d, 1H), 7.63(s, 1H), 8.11(d, 1H) Ig.1310 OCHF₂ Cl F CH₂—CO—OCH₃ CH₃—CH═C(Cl)— 105-107° C. Ik.1310 CF₃ Cl F CH₂—CO—OCH₃ CH₃ —CH═C(Cl)—3.82(s, 3H), 3.95(s, 3H), 4.08(s, 3H), 4.90(s, 2H), 7.32(d, 1H), 7.72(s,1H), 8.09(d, 1H) Ip.1094 OCHF₂ Cl F CH₂—CH═N—OCH₃ CH₃ —C≡C— 3.80-3.95(m,9H), 4.93 and 5.15(2d, together 2H), 6.72(t, 1H), 6.96 and 7.55(2t,together 1H), 7.31(d, 1H), 7.70 and 7.74(2d, together 1H)

Use Examples

The herbicidal activity of the substituted 3-phenylpyrazoles I wasdemonstrated by the following greenhouse experiments:

The culture containers used were plastic flowerpots containing loamysand with approximately 3.0% of humus as substrate. The seeds of thetest plant were sown separately for each species.

For the pre-emergence treatment, the active ingredients, suspended oremulsified in water, were applied directly after sowing by means offinely distributing nozzles. The contains were irrigated gently topromote germination and growth and subsequently covered with translucentplastic hoods until the plants had rooted. This cover caused uniformgermination of the test plants unless this was adversely affected by theactive ingredients.

For the post-emergence treatment, the test plants were grown to a plantheight of from 3 to 15 cm, depending on the plant habit, and only thentreated with the active ingredient which had been suspended oremulsified in water. To this end, the test plants were either sowndirectly and grown in the same containers, or they were first grownseparately as seedlings and transplanted into the test containers a fewdays prior to treatment. The rate of application for the post-emergencetreatment was 3.9 or 1.9 g/ha of a.s. (active substance).

Depending on the species, the plants were kept at from 10 to 25° C., or20-35° C., respectively. The test period extended over 2 to 4 weeks.During this time, the plants were tended, and their response to theindividual treatments was evaluated.

Evaluation was carried out using a scale of from 0 to 100. 100 means noemergence of the plants, or complete destruction of at least the aerialparts, and 0 means no damage, or normal course of growth.

The plants used in the greenhouse experiments belonged to the followingspecies:

Scientific name Common name Abutilon theophrasti velvet leaf Amaranthusretroflexus redroot pigweed Galium aparine catchweed bedstraw Sinapisalba white mustard Solanum nigrum black nightshade

At application rates of 3.9 and 1.9 g of a.s./ha post-emergence, thecompounds No. Ig.1310 and Ik.1310 showed a very good herbicidal activityagainst the abovementioned broad-leaved plants.

We claim:
 1. A 3-phenylpyrazole of formula I

in which the variables have the following meanings: R¹ is C₁-C₄-alkyl orC₁-C₄-haloalkyl; R² is cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl,C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkylthio, C₁-C₄-haloalkylthio,C₁-C₄-alkylsulfinyl, C₁-C₄-haloalkylsulfinyl, C₁-C₄-alkylsulfonyl, orC₁-C₄-haloalkylsulfonyl; R³ is hydrogen, cyano, halogen, C₁-C₄-alkyl orC₁-C₄-haloalkyl; R⁴ is hydrogen or halogen; R⁵ is cyano, halogen,C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy; R⁶, R⁷independently of one another are C₁-C₆-alkyl, C₁-C₆-haloalkyl,hydroxy-C₁-C₄-alkyl, cyano-C₁-C₄-alkyl, C₁-C₄-alkoxy-C₁-C₄-alkyl,C₁-C₄-haloalkoxy-C₁-C₄-alkyl, C₃-C₄-alkenyloxy-C₁-C₄-alkyl,C₃-C₄-alkynyloxy-C₁-C₄-alkyl, C₃-C₈-cycloalkoxy-C₁-C₄-alkyl,amino-C₁-C₄-alkyl, C₁-C₄-alkylamino-C₁-C₄-alkyl,di(C₁-C₄-alkyl)amino-C₁-C₄-alkyl, C₁-C₄-alkylthio-C₁-C₄-alkyl,C₁-C₄-haloalkylthio-C₁-C₄-alkyl, C₃-C₄-alkenylthio-C₁-C₄-alkyl,C₃-C₄-alkynylthio-C₁-C₄-alkyl, C₁-C₄-alkylsulfinyl-C₁-C₄-alkyl,C₁-C₄-haloalkylsulfinyl-C₁-C₄-alkyl, C₃-C₄-alkenylsulfinyl-C₁-C₄-alkyl,C₃-C₄-alkynylsulfinyl-C₁-C₄-alkyl, C₁-C₄-alkylsulfonyl-C₁-C₄-alkyl,C₁-C₄-haloalkylsulfonyl-C₁-C₄-alkyl, C₃-C₄-alkenylsulfonyl-C₁-C₄-alkyl,C₃-C₄-alkynylsulfonyl-C₁-C₄-alkyl, C₃-C₆-alkenyl, cyano-C₃-C₆-alkenyl,C₃-C₆-haloalkenyl, C₃-C₆-alkynyl, cyano-C₃-C₆-alkynyl,C₃-C₆-haloalkynyl, (C₁-C₄-alkyl)carbonyl, (C₁-C₄-haloalkyl)carbonyl,(C₁-C₄-alkoxy)carbonyl, aminocarbonyl, (C₁-C₄-alkyl)aminocarbonyl,di(C₁-C₄-alkyl)aminocarbonyl, (C₁-C₄-alkoxy-C₁-C₄-alkyl)carbonyl,C₁-C₄-alkylsulfonyl, C₁-C₄-haloalkylsulfonyl,(C₁-C₄-alkyl)carbonyl-C₁-C₄-alkyl,(C₁-C₄-haloalkyl)carbonyl-C₁-C₄-alkyl,(C₃-C₈-cycloalkyl)carbonyl-C₁-C₄-alkyl, (C₁-C₄-alkoxy)imino-C₁-C₄-alkyl,(C₃-C₄-alkenyloxy)imino-C₁-C₄-alkyl, hydroxycarbonyl-C₁-C₄-alkyl,(C₁-C₄-alkoxy)carbonyl-C₁-C₄-alkyl which is unsubstituted or substitutedby a (C₁-C₄-alkoxy)imino group, (C₁-C₄-haloalkoxy)carbonyl-C₁-C₄-alkyl,(C₁-C₄-alkylthio)carbonyl-C₁-C₄-alkyl, aminocarbonyl-C₁-C₄-alkyl,(C₁-C₄-alkylamino)carbonyl-C₁-C₄-alkyl,di(C₁-C₄-alkylamino)carbonyl-C₁-C₄-alkyl, C₃-C₈-cycloalkyl,C₃-C₈-cycloalkyl-C₁-C₄-alkyl, phenyl, phenyl-C₁-C₄-alkyl or 3- or7-membered heterocyclyl or heterocyclyl-C₁-C₄-alkyl, wherein one of thering members of the cycloalkyl rings and heterocycles optionally is acarbonyl or thiocarbonyl ring member; and wherein the cycloalkyl, phenyland heterocyclyl rings are unsubstituted or carry from one to foursubstituents selected from the group consisting of: cyano, nitro, amino,hydroxyl, carboxyl, halogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy,C₁-C₄-haloalkoxy, C₁-C₄-alkylthio, C₁-C₄-haloalkylthio,C₁-C₄-alkylsulfonyl, C₁-C₄-haloalkylsulfonyl, (C₁-C₄-alkoxy)carbonyl,(C₁-C₄-alkyl)carbonyl, (C₁-C₄-haloalkyl)carbonyl,(C₁-C₄-alkyl)carbonyloxy, (C₁-C₄-haloalkyl)carbonyloxy anddi(C₁-C₄-alkyl)amino; X is a chemical bond, a 1,2-ethynediyl group or agroup *—CH₂—CH(R⁸)— or *—CH═C(R⁸)— which is bonded to the phenyl ringvia the bond characterized with an asterisk, and wherein R⁸ is hydrogen,cyano, nitro, halogen, C₁-C₄-alkyl or C₁-C₄-haloalkyl; Y is oxygen orsulfur; or an agriculturally useful salt thereof.
 2. The3-phenylpyrazole defined in claim 1, or its agriculturally useful salt,wherein R¹ is C₁-C₄-alkyl.
 3. The 3-phenylpyrazole defined in claim 1,or its agriculturally useful salt, wherein R¹ is methyl.
 4. The3-phenylpyrazole defined in claim 1, or its agriculturally useful salt,wherein R² is trifluoromethyl, difluoromethoxy or methylsulfonyl.
 5. The3-phenylpyrazole defined in claim 1, or its agriculturally useful salt,wherein R² is difluoromethoxy.
 6. The 3-phenylpyrazole defined in claim1, or its agriculturally useful salt, wherein R³ is cyano or halogen. 7.The 3-phenylpyrazole defined in claim 1, or its agriculturally usefulsalt, wherein R³ is chlorine.
 8. The 3-phenylpyrazole defined in claim1, or its agriculturally useful salt, wherein R⁴ is fluorine orchlorine.
 9. The 3-phenylpyrazole defined in claim 1, or itsagriculturally useful salt, wherein R⁵ is chlorine.
 10. The3-phenylpyrazole defined in claim 1, or its agriculturally useful salt,wherein R⁶ is C₁-C₆-alkyl, C₁-C₆-haloalkyl, cyano-C₁-C₄-alkyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-alkylthio-C₁-C₄-alkyl,C₁-C₄-alkylsulfonyl-C₁-C₄-alkyl, C₃-C₆-alkenyl, C₃-C₆-haloalkenyl,C₃-C₆-alkynyl, (C₁-C₄-alkyl)carbonyl, (C₁-C₄-haloalkyl)carbonyl,(C₁-C₄-alkoxy)carbonyl, di(C₁-C₄-alkyl)aminocarbonyl,(C₁-C₄-alkyl)carbonyl-C₁-C₄-alkyl,(C₃-C₈-cycloalkyl)carbonyl-C₁-C₄-alkyl, (C₁-C₄-alkoxy)imino-C₁-C₄-alkyl,hydroxycarbonyl-C₁-C₄-alkyl, (C₁-C₄-alkoxy)carbonyl-C₁-C₄-alkyl which isunsubstituted or substituted by a (C₁-C₄-alkoxy)imino group,di(C₁-C₄-alkyl)aminocarbonyl-C₁-C₄-alkyl, C₃-C₈-cycloalkyl,C₃-C₈-cycloalkyl-C₁-C₄-alkyl or phenyl-C₁-C₄-alkyl.
 11. The3-phenylpyrazole defined in claim 1, or its agriculturally useful salt,wherein R⁶ is a C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-alkynyl,(C₁-C₄-alkyl)carbonyl, (C₁-C₄-alkoxy)carbonyl,di(C₁-C₄-alkyl)aminocarbonyl, (C₁-C₄-alkoxy)carbonyl-C₁-C₄-alkyl ordi(C₁-C₄-alkyl)aminocarbonyl-C₁-C₄-alkyl.
 12. The 3-phenylpyrazoledefined in claim 1, or its agriculturally useful salt, wherein R⁷ isC₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-alkynyl,(C₁-C₄-alkoxy)carbonyl-C₁-C₄-alkyl or phenyl-C₁-C₄-alkyl.
 13. The3-phenylpyrazole defined in claim 1, or its agriculturally useful salt,wherein X is a chemical bond, a 1,2-ethynediyl group or a group*—CH═C(R⁸)—, wherein R⁸ is hydrogen, cyano, chlorine, bromine or methyl.14. The 3-phenylpyrazole defined in claim 13, or its agriculturallyuseful salt, wherein R⁸ is chlorine.
 15. The 3-phenylpyrazole defined inclaim 1, or its agriculturally useful salt, wherein X is a chemicalbond.
 16. The 3-phenylpyrazole defined in claim 1, or its agriculturallyuseful salt, wherein Y is oxygen.
 17. A herbicidal compositioncomprising a herbicidally active amount of at least one 3-phenylpyrazoleas defined in claim 1 or of an agriculturally useful salt thereof and atleast one liquid or solid carrier.
 18. The composition defined in claim17, further comprising at least one surfactant.
 19. A process for thepreparation of the 3-phenylpyrazole defined in claim 1, which comprisesreacting an alkoxyamide of formula III

with an alkylating or acrylating agent L-R⁶, wherein L is a leavinggroup, in the presence of a base.
 20. A method of controllingundesirable vegetation, which comprises treating plants, theirenvironment or seeds with a herbidically active amount of at least one3-phenylpyrazole as defined in claim 1 or of an agriculturally usefulsalt thereof.